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GENERAL CLINICS
 Master. Idriss 3 ½ years /Mch
 DOB – 11/7/19 .
 Informant – mother ; reliability – good.
 From Washermanpet .
 First born to NCM parents, brought with complaints of not
attaining age appropriate milestones noticed by the mother
since 8 months of age.
ANTENATAL HISTORY
 Menarche @ 13 years, Regular cycles
 LMP : 25.11.2018 ; EDD : 2.9.1019
 Mother got married at 20 years of age.
 Conceived in the same year (spontaneous )
 No previous miscarriages
 Pregnancy confirmed by UPT at around 45 days of
amenorrhoea.
FIRST TRIMESTER
 Registered in nearby PHC.
 Immunised with 2 doses of TT.
 Dating scan done at 8 weeks – Normal.
 No h/o any chronic drug intake.
 No h/o irradiation
 No h/o fever with rash , joint pain ,painful swellings behind
the ear , pets at home
 No h/o excessive vomiting requiring hospitalisation .
 No h/o bleeding / draining PV .
SECOND TRIMESTER
 Took IFA regularly.
 Quickening felt at around 5 months of gestation .
 AN Scans – Anomaly scan said to be normal
Low lying placenta + , advised bedrest.
 h/o PIH diagnosed at 7 months and started on oral
medication .
 No h/o GDM , Epilepsy, UTI , thyroid dysfunction , foul
smelling vaginal discharge.
 No h/o bleeding / draining PV
THIRD TRIMESTER
 Continued to perceive fetal movements
 No history s/o malpresentation or abnormal lie.
 Around 32 weeks of gestation , She was admitted in IOG with
complaints of abdominal pain & draining PV . Hospitalised for 7
days . Saline infusion given vaginally and then discharged on
8.7.2019
 No bleeding PV
 No h/o Fever with rash, GDM, Epilepsy, Thyroid disorders, Foul
smelling vaginal discharges, Blood transfusions
 Weight gain – 10 kg.
NATAL HISTORY
 On the next day of discharge, she developed severe headache , vomiting
and was again admitted in IOG. She was found to have increased BP ,
advised for termination of pregnancy for the sake of the mother .
 Labour was induced on 9/7/19 – 1st with a tube , then with a gel kept
vaginally .
 Developed labour pains at around 7 pm on 10/7/19
 Delivered a live male baby ( preterm ) on 11/7/19 around 5 am
 Baby cried immediately at birth .
 Birth weight : 1.750 kg
 Was then shifted to NICU
NEONATAL HISTORY
 Baby was admitted for preterm /LBW care in NICU.
 Mother saw the baby on day 3 of life she was informed that the baby is a preterm/ LBW and
adequate care must be taken.
 On day 3 of life, baby on oxygen support via nasal cannula.
 Feeds started through tube in mouth from 4 th day.
 Baby was kept in blue light for jaundice from 5th to 7 th day.
 From day 5 of life , baby developed abdominal distension and vomiting
 Mother was informed that the baby developed some abdominal infection and feeds should be
stopped & IV fluids and IV medications given , baby kept NPO for 1 week. Gradually abdominal
distension reduced ; tube feeds restarted from day 15 of life.
 No h/o neonatal seizures / hypoglycemia / bleeding manifestations.
 Baby was not able to suck properly and hence paladai feeds were taught to the mother. KMC
care were taught.
 Discharged after 25 days of NICU stay with supplements.
 Discharge weight : 1.700 kg
Postnatal history
 H/o poor sucking present
 Confined with paladai feeds till 3 months of age & DBF given till 1 year of
age.
 No h/o seizures, hypoglycemia, bleeding manifestations.
HISTORY OF PRESENTING ILLNESS
DEVELEOPMENTAL DELAY AND MOTOR PROBLEMS
 Since this was her 1st child and she was not aware of normal development
milestones , she thought her child was normal.
 She became concerned only at 8 months of age when the child did not attain
head control and has no social smile.
 She also noticed that her child always keeps his legs straight and stiff.
 H/o scissoring of both lower limbs present and she found it difficult to change
diapers.
 He also keeps his hands closed tightly most of the time.
 Child was not very active and reduced movements in all 4 limbs (LL>UL)
 For the above complaints , he was initially taken to ICH . He was admitted and investigations
done.
 Mother was informed that her child had brain damage and developmental delay . The disease is
not curable and but can be improved with physiotherapy and advised regular follow up.
 Then lost follow up in ICH. He was brought to Stanley at 1 year 3 months of age , was registered in
our DEIC and is on regular follow up since then.
 Child is aware of surroundings
 Child recognises mother & responds to mother when called.
 Child will be interested in surrounding & plays with toys well & Looks into objects when shown.
 Child able to speak one or 2 word meaningful words to the mother.
 No h/o violent behaviours /sleep disturbances
 Able to appreciate smell
 Able to identify alphabets and different colours.
 h/o deviation of right eye towards midline, noticed by the mother since early infancy.
 No h/o loss of sensation of face.
 No h/o difficulty in closing the eyes while sleeping , no h/o facial asymmetry
 He turns to the side of sound stimuli.
 h/o drooling of saliva from early infancy.
 h/o recurrent episodes of aspiration with regurgitation of feeds since infancy. No
h/o voice change
 No h/o difficulty in turning head side to side.
 No h/o difficulty in protruding tongue.
 Child always keeps his legs straight and stiff.
 H/o difficulty in lifting head above the bed & getting up from sitting and lying positions
 H/o difficulty in turning to one side from lying posture.
 H/o difficulty in holding objects in hands
 H/o tightness noted in all 4 limbs (LL>UL) since early infancy & h/o scissoring of both
lower limbs present, it was difficult to change diapers.
 H/o weakness in all 4 limbs (LL>UL)
 Can’t able to walk normally.
 Able to appreciate clothes over his body
 Able to differentiate hot and cold water,
 Cries during immunisation .
 No head nodding , abnormal eye movements .
 No h/o tremors.
 No h/o involuntary movements.
 No h/o bowel bladder incontinence @ present
 No h/o flushing of skin, excessive sweating
 No h/o bed sores / constipation
 No h/o sleep disturbances / incessant cry.
 No h/o spinal deformities.
 H/o seizures – 3 episodes, from 2 years 3 months of age in the form of tonic
clonic movements of left upper limb , lower limb. For every episodes, child
got admitted in ISP and treated with IV medications & oral drugs
 Now the child is on 2 AED syrup , compliance is good and is on regular follow
up in paed neuro OPD. Currently, child is seizure free for last 1 year.
 Mother feels her child is not gaining adequate weight and height compared
with peers
 h/o recurrent RTI present – treated on OPD basis.
 No h/o previous blood transfusions.
DEVELOPMENT HISTORY
GROSS MOTOR EXAMINATION
Head control – 1 year 8 months
Rolls over - 1 year 10 months.
Sits with support – 2 and half years.
Sits without support – 2 years 8 months.
Stands with support – 3 years.
Developmental age : 1 year
DQ : 33
FINE MOTOR EXAMINATION
Bidextrous grasp – 2 yrs
Uni dextrous grasp – 2 yr 3 months
Transfers objects -2 and half years.
Holds chalk , scribbles – 3 years.
Draws line - 3 and half years.
Developmental age : 1 ½ years
DQ : 50
SOCIAL
social smile – 5 months
Bye bye – 1 year.
Interacts with peers – 2 years.
Asks for food, drink – 2 ½ years
LANGUAGE
Cooing – 4 months
Monosyllable – 8 months
Bisyllable – 1 year 2 months.
3- 6 words – 1 and half years.
2 word sentences – 2 years.
Tell name & rhymes – 3 years.
Currently child is on regular follow up in DEIC, ISP for Physiotherapy , Speech
therapy & Occupational therapy. Child’s symptoms gradually improving after
starting therapies.
Now at 3 and half years , he is
 Able to lift head up when lying supine.
 Able to get up from lying position with one elbow supported.
 Able to sit without support and stands with support for few minutes.
 Able to lift his arms above head , and is able to take food to his mouth
without difficulty .
 Able to take tiny objects with two fingers in both hands
 Tightness in extremities improving and drooling of saliva from mouth have
became better.
 No history of regression of previously attained milestones.
DIET HISTORY
 Exclusive breast feeding till 1 year , Complemetary feeds started only after 1
year .
 Now child consumes mixed diet with predominant vegetarian based diet.
Expected Child taking Deficit
Calories 1250 k cal 720 k cal 530 k cal
proteins 22 gm 15 gm 7 gm
IMMUNISATION HISTORY
Immunised upto age according to National Immunization schedule .
Last vaccination at 1 and half years.
FAMILY HISTORY
Non consanguinous marriage.
Single child to the mother.
No h/o development delay in family.
No h/o seizure disorder.
No family h/o early infant death .
SOCIOECONOMIC STATUS
Mother – VIII , Housewife
Father – X , Doing own business earning 15000/ month
Lower middle class.
ALLERGY HISTORY / CONTACT HISTORY : Nil significant
SUMMARY
 3 ½ years old 1st male child born to NCM parents who is a NICU
graduate (preterm / LBW with Complications- NEC /
 Now brought with predominant motor delay and stiffness of all 4 limbs
(LL > UL), improving with physiotherapy with right eye squint and
drooling of saliva with seizure disorder , probably a case of cerebral
palsy , I would like to to proceed with examination to confirm my
diagnosis and to localise the lesion .
GENERAL EXAMINATION
 Child is alert , looks around , interested in surroundings .
 Afebrile
 Hydration adequate
 Not anaemic / icteric
 No cyanosis / clubbing
 No pedal edema / significant generalised lymphadenopathy.
 VITALS :
PR – 100, Regular in rhythm, Normal volume, No specific character, No RR or RF
delay
RR- 24/min, Abdominothoracic type
BP – 90/60 mm hg, measured in right upper arm in sitting position
TEMP – 98.4 F
Spo2 : 98 % in room air
ANTHROPOMETRY
 HEIGHT : 89 cms- < 3rd percentile
 WEIGHT :9 kg  < 3rd percentile
 HEAD CIRCUMFERENCE : 45 cms  < 3rd percentile
 MIDARM CIRCUMFERENCE :14 cms
 WEIGHT for HEIGHT : < -3 SD
HEAD TO FOOT EXAMINATION
 Head – shape normal , microcephaly present. AP/PF – closed , No over riding of
sutures.
 Hair – normal
 Face – no dysmorphic facies
 Eyes – right eye squint , no cataract / nystagmus /ptosis. No signs of vitamin A
deficiency.
 Ears – normal ; no discharge
 Mouth – no cleft lip/palate
no ulcers , no thrush / caries.
drooling of saliva present
 Neck – normal
 Chest/ abdomen - normal
 Spine – no kyphoscoliosis.
 Limbs – no deformities / contractures
 No bedsore / callus
 Skin – No neurocutaneous markers.
 BCG scar : present
CENTRAL NERVOUS SYSTEM EXAMINATION
HIGHER FUNCTIONS
Alert , interested in surroundings, Looks at the examiner while examining
Speech and language – Understands commands, comprehension present , replies in
sentences of 3-4 words, pronounciation – Not clear.
Memory – able to recollect immediate and recent memory
Intelligence – not tested
CRANIAL NERVES EXAMINATION
 1 – Not tested
 2 – Able to follow and fix objects , BPERL +
Direct and indirect Light reflex – present
Fundus : not cooperative
 3, 4, 6 – right eye convergent squint + , Able to follow objects ; no nystagmus.
 5 – sensation over face – Present ; able to chew food ; Jaw jerk ++
 7 –able to close eyes tightly , no deviation of angle of mouth while talking/smiling ; No obvious
facial asymmetry ; Drooling of saliva present on right side
 8 – Turns to the side of sounds ; understands and responds to speech ,
 9,10- Uvula in midline ; Gag reflex – not tested
 11- able to turn head side to side.
 12-able to protrude tongue outside . No deviation .
MOTOR SYSTEM
Examined with the patient on the couch in supine position
POSTURE – both LL extended and UL flexed.
Ankle dorsiflexed
BULK – RIGHT LEFT
Upper arm 14 cms 14cms
Upper thigh 22cms 22 cms
TONE
RIGHT LEFT
UPPER LIMB -
LOWER LIMB -
POWER
UPPER LIMB - 4/5 4/5
LOWER LIMB - 3/5 3/5
REFLEXES
Abdominal reflex + on both sides
Conjunctival reflex + on both sides
RIGHT LEFT
Biceps ++ ++
Triceps ++ ++
Supinator ++ ++
Knee +++ +++
Ankle +++ +++
B/L plantar Extensors
No Clonus
No primitive reflexes.
SENSORY
Pain , pressure and temperature – intact bilaterally
Joint position and vibration – not done
CEREBELLAR
No hypotonia , nystagmus , intentional tremors , Pendular knee
jerk.
No involuntary movements .
No signs of ANS dysfunction.
No kyphoscoliosis
No signs of meningeal irritation.
OTHER SYSTEMS - Normal
SUMMARY
 3 ½ years old male child – 1st born NCM ; NICU graduate – 25 days NICU stay .
Preterm / LBW
 Presenting with predominant motor delay on physiotherapy , non progressive ,no
regression of milestones.
 Seizure disorder – on AED
 EXAMINATION REVEALED – spasticity of all limbs , LL > UL , exaggerated DTR , no
involuntary movements.
 Right eye squint , normal vision & hearing
DIAGNOSIS
 A case of Static encephalopathy, spastic diplegia cerebral palsy – ( LL
> UL ), GMFCS – IV
 Associated with seizure disorder., right eye squint.
 Chronic malnutrition , apparently normal vision & hearing.
 Probable etiology being – Preterm / hypoxic insult / postnatal
infection .

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cerebral palsy - case presentation ^.pptx

  • 2.  Master. Idriss 3 ½ years /Mch  DOB – 11/7/19 .  Informant – mother ; reliability – good.  From Washermanpet .  First born to NCM parents, brought with complaints of not attaining age appropriate milestones noticed by the mother since 8 months of age.
  • 3. ANTENATAL HISTORY  Menarche @ 13 years, Regular cycles  LMP : 25.11.2018 ; EDD : 2.9.1019  Mother got married at 20 years of age.  Conceived in the same year (spontaneous )  No previous miscarriages  Pregnancy confirmed by UPT at around 45 days of amenorrhoea.
  • 4. FIRST TRIMESTER  Registered in nearby PHC.  Immunised with 2 doses of TT.  Dating scan done at 8 weeks – Normal.  No h/o any chronic drug intake.  No h/o irradiation  No h/o fever with rash , joint pain ,painful swellings behind the ear , pets at home  No h/o excessive vomiting requiring hospitalisation .  No h/o bleeding / draining PV .
  • 5. SECOND TRIMESTER  Took IFA regularly.  Quickening felt at around 5 months of gestation .  AN Scans – Anomaly scan said to be normal Low lying placenta + , advised bedrest.  h/o PIH diagnosed at 7 months and started on oral medication .  No h/o GDM , Epilepsy, UTI , thyroid dysfunction , foul smelling vaginal discharge.  No h/o bleeding / draining PV
  • 6. THIRD TRIMESTER  Continued to perceive fetal movements  No history s/o malpresentation or abnormal lie.  Around 32 weeks of gestation , She was admitted in IOG with complaints of abdominal pain & draining PV . Hospitalised for 7 days . Saline infusion given vaginally and then discharged on 8.7.2019  No bleeding PV  No h/o Fever with rash, GDM, Epilepsy, Thyroid disorders, Foul smelling vaginal discharges, Blood transfusions  Weight gain – 10 kg.
  • 7. NATAL HISTORY  On the next day of discharge, she developed severe headache , vomiting and was again admitted in IOG. She was found to have increased BP , advised for termination of pregnancy for the sake of the mother .  Labour was induced on 9/7/19 – 1st with a tube , then with a gel kept vaginally .  Developed labour pains at around 7 pm on 10/7/19  Delivered a live male baby ( preterm ) on 11/7/19 around 5 am  Baby cried immediately at birth .  Birth weight : 1.750 kg  Was then shifted to NICU
  • 8. NEONATAL HISTORY  Baby was admitted for preterm /LBW care in NICU.  Mother saw the baby on day 3 of life she was informed that the baby is a preterm/ LBW and adequate care must be taken.  On day 3 of life, baby on oxygen support via nasal cannula.  Feeds started through tube in mouth from 4 th day.  Baby was kept in blue light for jaundice from 5th to 7 th day.  From day 5 of life , baby developed abdominal distension and vomiting  Mother was informed that the baby developed some abdominal infection and feeds should be stopped & IV fluids and IV medications given , baby kept NPO for 1 week. Gradually abdominal distension reduced ; tube feeds restarted from day 15 of life.  No h/o neonatal seizures / hypoglycemia / bleeding manifestations.  Baby was not able to suck properly and hence paladai feeds were taught to the mother. KMC care were taught.  Discharged after 25 days of NICU stay with supplements.  Discharge weight : 1.700 kg
  • 9. Postnatal history  H/o poor sucking present  Confined with paladai feeds till 3 months of age & DBF given till 1 year of age.  No h/o seizures, hypoglycemia, bleeding manifestations.
  • 10. HISTORY OF PRESENTING ILLNESS DEVELEOPMENTAL DELAY AND MOTOR PROBLEMS  Since this was her 1st child and she was not aware of normal development milestones , she thought her child was normal.  She became concerned only at 8 months of age when the child did not attain head control and has no social smile.  She also noticed that her child always keeps his legs straight and stiff.  H/o scissoring of both lower limbs present and she found it difficult to change diapers.  He also keeps his hands closed tightly most of the time.  Child was not very active and reduced movements in all 4 limbs (LL>UL)
  • 11.  For the above complaints , he was initially taken to ICH . He was admitted and investigations done.  Mother was informed that her child had brain damage and developmental delay . The disease is not curable and but can be improved with physiotherapy and advised regular follow up.  Then lost follow up in ICH. He was brought to Stanley at 1 year 3 months of age , was registered in our DEIC and is on regular follow up since then.  Child is aware of surroundings  Child recognises mother & responds to mother when called.  Child will be interested in surrounding & plays with toys well & Looks into objects when shown.  Child able to speak one or 2 word meaningful words to the mother.  No h/o violent behaviours /sleep disturbances  Able to appreciate smell  Able to identify alphabets and different colours.  h/o deviation of right eye towards midline, noticed by the mother since early infancy.  No h/o loss of sensation of face.  No h/o difficulty in closing the eyes while sleeping , no h/o facial asymmetry
  • 12.  He turns to the side of sound stimuli.  h/o drooling of saliva from early infancy.  h/o recurrent episodes of aspiration with regurgitation of feeds since infancy. No h/o voice change  No h/o difficulty in turning head side to side.  No h/o difficulty in protruding tongue.  Child always keeps his legs straight and stiff.  H/o difficulty in lifting head above the bed & getting up from sitting and lying positions  H/o difficulty in turning to one side from lying posture.  H/o difficulty in holding objects in hands  H/o tightness noted in all 4 limbs (LL>UL) since early infancy & h/o scissoring of both lower limbs present, it was difficult to change diapers.  H/o weakness in all 4 limbs (LL>UL)  Can’t able to walk normally.
  • 13.  Able to appreciate clothes over his body  Able to differentiate hot and cold water,  Cries during immunisation .  No head nodding , abnormal eye movements .  No h/o tremors.  No h/o involuntary movements.  No h/o bowel bladder incontinence @ present  No h/o flushing of skin, excessive sweating  No h/o bed sores / constipation  No h/o sleep disturbances / incessant cry.  No h/o spinal deformities.
  • 14.  H/o seizures – 3 episodes, from 2 years 3 months of age in the form of tonic clonic movements of left upper limb , lower limb. For every episodes, child got admitted in ISP and treated with IV medications & oral drugs  Now the child is on 2 AED syrup , compliance is good and is on regular follow up in paed neuro OPD. Currently, child is seizure free for last 1 year.  Mother feels her child is not gaining adequate weight and height compared with peers  h/o recurrent RTI present – treated on OPD basis.  No h/o previous blood transfusions.
  • 15. DEVELOPMENT HISTORY GROSS MOTOR EXAMINATION Head control – 1 year 8 months Rolls over - 1 year 10 months. Sits with support – 2 and half years. Sits without support – 2 years 8 months. Stands with support – 3 years. Developmental age : 1 year DQ : 33 FINE MOTOR EXAMINATION Bidextrous grasp – 2 yrs Uni dextrous grasp – 2 yr 3 months Transfers objects -2 and half years. Holds chalk , scribbles – 3 years. Draws line - 3 and half years. Developmental age : 1 ½ years DQ : 50
  • 16. SOCIAL social smile – 5 months Bye bye – 1 year. Interacts with peers – 2 years. Asks for food, drink – 2 ½ years LANGUAGE Cooing – 4 months Monosyllable – 8 months Bisyllable – 1 year 2 months. 3- 6 words – 1 and half years. 2 word sentences – 2 years. Tell name & rhymes – 3 years.
  • 17. Currently child is on regular follow up in DEIC, ISP for Physiotherapy , Speech therapy & Occupational therapy. Child’s symptoms gradually improving after starting therapies. Now at 3 and half years , he is  Able to lift head up when lying supine.  Able to get up from lying position with one elbow supported.  Able to sit without support and stands with support for few minutes.  Able to lift his arms above head , and is able to take food to his mouth without difficulty .  Able to take tiny objects with two fingers in both hands  Tightness in extremities improving and drooling of saliva from mouth have became better.  No history of regression of previously attained milestones.
  • 18. DIET HISTORY  Exclusive breast feeding till 1 year , Complemetary feeds started only after 1 year .  Now child consumes mixed diet with predominant vegetarian based diet. Expected Child taking Deficit Calories 1250 k cal 720 k cal 530 k cal proteins 22 gm 15 gm 7 gm
  • 19. IMMUNISATION HISTORY Immunised upto age according to National Immunization schedule . Last vaccination at 1 and half years. FAMILY HISTORY Non consanguinous marriage. Single child to the mother. No h/o development delay in family. No h/o seizure disorder. No family h/o early infant death . SOCIOECONOMIC STATUS Mother – VIII , Housewife Father – X , Doing own business earning 15000/ month Lower middle class. ALLERGY HISTORY / CONTACT HISTORY : Nil significant
  • 20. SUMMARY  3 ½ years old 1st male child born to NCM parents who is a NICU graduate (preterm / LBW with Complications- NEC /  Now brought with predominant motor delay and stiffness of all 4 limbs (LL > UL), improving with physiotherapy with right eye squint and drooling of saliva with seizure disorder , probably a case of cerebral palsy , I would like to to proceed with examination to confirm my diagnosis and to localise the lesion .
  • 21. GENERAL EXAMINATION  Child is alert , looks around , interested in surroundings .  Afebrile  Hydration adequate  Not anaemic / icteric  No cyanosis / clubbing  No pedal edema / significant generalised lymphadenopathy.  VITALS : PR – 100, Regular in rhythm, Normal volume, No specific character, No RR or RF delay RR- 24/min, Abdominothoracic type BP – 90/60 mm hg, measured in right upper arm in sitting position TEMP – 98.4 F Spo2 : 98 % in room air
  • 22. ANTHROPOMETRY  HEIGHT : 89 cms- < 3rd percentile  WEIGHT :9 kg  < 3rd percentile  HEAD CIRCUMFERENCE : 45 cms  < 3rd percentile  MIDARM CIRCUMFERENCE :14 cms  WEIGHT for HEIGHT : < -3 SD
  • 23.
  • 24. HEAD TO FOOT EXAMINATION  Head – shape normal , microcephaly present. AP/PF – closed , No over riding of sutures.  Hair – normal  Face – no dysmorphic facies  Eyes – right eye squint , no cataract / nystagmus /ptosis. No signs of vitamin A deficiency.  Ears – normal ; no discharge  Mouth – no cleft lip/palate no ulcers , no thrush / caries. drooling of saliva present  Neck – normal  Chest/ abdomen - normal
  • 25.  Spine – no kyphoscoliosis.  Limbs – no deformities / contractures  No bedsore / callus  Skin – No neurocutaneous markers.  BCG scar : present CENTRAL NERVOUS SYSTEM EXAMINATION HIGHER FUNCTIONS Alert , interested in surroundings, Looks at the examiner while examining Speech and language – Understands commands, comprehension present , replies in sentences of 3-4 words, pronounciation – Not clear. Memory – able to recollect immediate and recent memory Intelligence – not tested
  • 26. CRANIAL NERVES EXAMINATION  1 – Not tested  2 – Able to follow and fix objects , BPERL + Direct and indirect Light reflex – present Fundus : not cooperative  3, 4, 6 – right eye convergent squint + , Able to follow objects ; no nystagmus.  5 – sensation over face – Present ; able to chew food ; Jaw jerk ++  7 –able to close eyes tightly , no deviation of angle of mouth while talking/smiling ; No obvious facial asymmetry ; Drooling of saliva present on right side  8 – Turns to the side of sounds ; understands and responds to speech ,  9,10- Uvula in midline ; Gag reflex – not tested  11- able to turn head side to side.  12-able to protrude tongue outside . No deviation .
  • 27. MOTOR SYSTEM Examined with the patient on the couch in supine position POSTURE – both LL extended and UL flexed. Ankle dorsiflexed BULK – RIGHT LEFT Upper arm 14 cms 14cms Upper thigh 22cms 22 cms TONE RIGHT LEFT UPPER LIMB - LOWER LIMB - POWER UPPER LIMB - 4/5 4/5 LOWER LIMB - 3/5 3/5
  • 28. REFLEXES Abdominal reflex + on both sides Conjunctival reflex + on both sides RIGHT LEFT Biceps ++ ++ Triceps ++ ++ Supinator ++ ++ Knee +++ +++ Ankle +++ +++ B/L plantar Extensors No Clonus No primitive reflexes. SENSORY Pain , pressure and temperature – intact bilaterally Joint position and vibration – not done
  • 29. CEREBELLAR No hypotonia , nystagmus , intentional tremors , Pendular knee jerk. No involuntary movements . No signs of ANS dysfunction. No kyphoscoliosis No signs of meningeal irritation. OTHER SYSTEMS - Normal
  • 30. SUMMARY  3 ½ years old male child – 1st born NCM ; NICU graduate – 25 days NICU stay . Preterm / LBW  Presenting with predominant motor delay on physiotherapy , non progressive ,no regression of milestones.  Seizure disorder – on AED  EXAMINATION REVEALED – spasticity of all limbs , LL > UL , exaggerated DTR , no involuntary movements.  Right eye squint , normal vision & hearing
  • 31. DIAGNOSIS  A case of Static encephalopathy, spastic diplegia cerebral palsy – ( LL > UL ), GMFCS – IV  Associated with seizure disorder., right eye squint.  Chronic malnutrition , apparently normal vision & hearing.  Probable etiology being – Preterm / hypoxic insult / postnatal infection .