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SYNDROMESDR NIVYA SHETTY(GOVT.DENTAL COLLEGE AND HOSPITAL,MUMBAI)
PARRY
ROMBERG
SYNDROME
Facial
hemiatrophy
VANDER
WOUDE
SYNDROME
pits of lower lip
cleft of palate
ASCHERS
SYNDROME
Double lip
Brephalochelasis
Non toxic
thyroidenlargement
MELKERSON
ROSENTHAL
SYNDROME
Cheilitis granulomatosa
Scrotal tongue
Facial paralysis
PEUTZ
JEGHERS
SYNDROME
Pigmentation of face, oral
cavity ,hands
Multiple intestinal polyposis
RUBINSTEIN TAYBI
SYNDROME
Talons cusp
Developmental
retardation
Broad thumbs and
toes
Incomplete or no
descent of testes
KLINEFELTER
SYNDROME(TRIS
OMY 46)
xxy
taurodontism
GARDNERS SYNDROM
supernumerary tooth
multiple int. polyposis
multiple sebaceous cyst
osteoma
LADD
SYNDROME
Lacrimla gland
inflammation and
aplasia
Auricle deformity
Dental:peg ,enamel
hypoplasia,hypodontia
Digital
deformity:clinodactyly
BECKWITH
WIEDEMAN
SYNDROME
Macroglosia
Microcephaly
Neonatal
hypoglycaemia
Fetal visceromegaly
BENINGN AND
MALIGNANT TUMORS
COWDENS
SYNDROME
Oral papillomatous
lesion
Facial trichilemmomas
associated with git
Thyroid
Cns abnormalities
SYNDROME/
DYSPLASTIC
NEVUS
SYNDROME
Large
pigmentation
High risk of
melanoma
1(MULTIPLE
ENDOCRINE
NEOPLASIA
SYNDROME)
Hyperplasia of
Pituitory
Parathyroid
Adrenal cortex
Pancreatic islets
MENS 2(SIPPLE
SYNDROME)
Parathyroid
hypoplasia
Pheochromocytoma
Medullary carcinoma
of thyroid
SALIVARY GLAND
TUMORS
SJOGRENS
SYNDROME
Keratoconjunctivitis
sicca
Xerostomia
Rheumatoid arthritis
CYST AND TUMOR OF
ODONTOGENIC ORIGIN
GORLIN
GOLTZ/JAW CYST
CELL NEVUS/BIFID
RIB SYNDROME
Multiple odontogenic
keratocyst
Basal cell carcinoma
Bifid basal rib
Neurologic, sexual,
opthalmalogic
abnormality
Bilamellar calcification of
falx cerebri
BACTERIAL,VIRAL,MYCOTIC INFECTIONS
HEERFORD
T
SYNDROME
Uveoparotid fever
Associated with
facial palsy
BEHCETS
SYNDROME
Oral ulcer
Genital ulcer
Ocular
inflammation
REITERS
SYNDROME
Oral ulcer
urethritis
Arthritis
conjunctivitis
RAMSAY HUNT
SYNDROME
Herpes zoster
infection of
geniculate
ganglion with
Involvement of ext
ear and oral
mucosa
DISEASE OF BONES AND JOINTS
CROUZON
SYNDROME/
CRANIOFACIAL
DYSOSTOSIS
Prognathic mandible
Hypoplastic maxilla
High arched palate
Parrot beak
appearance
Hypertelorismi.e increased
distance between two structures here
eyes
APERT
SYNDROME
Syndactyly
(mitten hands and
sock feet)
Features of crouzon
syndrome
TREACHER
COLLINS
SYNDROME/
MADIBULOFACIAL
DYSOSTOSIS/
FRANSCHETTI
SYNDROME
Hypoplasia of mandible
and malar bone
Malformation of
external ear
High arched palate
Bird or fish like face
Antimongoloid slant
Coloboma of lower
PIERRE ROBIN
SYNDROME
Cleft palate
Micrognathia
glossoptosis
ALBRIGHT
SYNDROME
Precocious puberty
Polyostotic fibrosis
Café au lait
pigmentation
MARFAN
SYNDROME
Long thin extremeties
Hyper extensibility of
joints
Spidery
finger/arachnodactyly
Biifid uvula
Cvs complication
DOWN
SYNDROME
(TRISOMY21,
ONGOLISM)
Macroglosia
Flat face
Large anterior fontanelle
Hypermobility
Sexual and cardiac
abnormality
VAN BUCHEM
SYNDROME
Generalised cortical
hyperostosis
GORHAM
SYNDROME
Massive osteolysis or
vanishing bone
CAFFEY
SILVERMANN
SYNDROME
Infantile cortical
hyperostosis
Dysphagia
Hyperirritabity
Increased alkaline
phosphatase
COSTEN
SYNDROME
Tinnitus
Otalgia
Headache
Dizziness
Burning throat and
tongue
MPDS
Masticatory muscle
tenderness,pain,
limitation of motion,
clicking or propping sound
DISEASE OF BLOOD
FANCONI
SYNDROME
Aplastic anemia
Microcephaly
Hypogenitalism
Olive brown
pigmentation
PLUMMER VINSON
SYNDROME
Iron deficiency anemia
Carcinoma of hypopharynx
Koilonychia
Angular stomatitis
WISKOTT
ALDRICH
SYNDROME
Thrombocytopenic
purpura
Eczema
Increased susceptibility
to infection
CHEDIAK HIGASHI
SYNDROME
Malignant lymphoma
Albinism
Nystagmus
Recurrent infection
Photophobia
gingivitis
glossitis
KOSTMANN
SYNDROME
Severe congenital
neutropenia
DISEASE OF PERIODONTIUM
PAPILLON LEFEVRE
SYNDROME
Juvenile periodontitis
Palmar plantar keratosis
Calcificaton of falx cerebri
SKIN DISEASE
STEVEN JOHNSON
SYNDROME
Erythema
multiforme(severe
bullous form)
Skin,eyes,oral
cavity,genitelia
CREST SYNDROME
Calcinosis cutis
Raynods phenomena
Esophageal dysfunction
Sclero dactyly
telengectesia
EHLER DANLOS
SYNDROME
Hyperextension of
joints
Hypermobility of
tmj(rubber man)
GOLTZ GORLIN
SYNDROME
(focal dermal
hypoplasia)
Multi papillomas
Atrophy of skin
Polydactyly
Sunken eye
Sparse hair
GRINSPAN
SYNDROME
Lichen planus
Vascular hypertension
Diabetes mellitus
DISEASE OF NERV ES AND MUSCLES
RAEDERS
SYNDROME
(para trigeminal
syndrome)
Severe headache
Ocular sympathetic paralysis
FREYS SYNDROME
(auriculotemporal
syndrome)
Gustatory sweating
HORNERS
SYNDROME
Ptosis
Miosis
Anhidrosis
Enopthalmos
Vasodilation
JAW WINKING
SYNDROME/MARCUS
GUN PHENOMENA
Ptosis
Rapid elevation of ptotic
eye lid on moving jaw to
contralateral side
TROTTERS
SYNDROME
Tumors of nasopharynx
producing pain same as
trigeminl neuralgia
Middle ear deafness
EAGLES
SYNDROME(calcification of
stylohyoid ligament)
Dysphagia
Sore throat
Otalgia
glossodynia
FLOPPY INFANT
SYNDROME
Hypotonia
Inability to stand sit and walk
MOBIUS SYNDROME
Partial/complete paralysis of
face
Drooling of saliva
Difficulty in mastication
Congenital facial dysplegia
HORTONS
SYNDROME
Vascular headache
ORAL ASPECTS OF METABOLIC DISEASE
CUSHING
SYNDROME
Hyperadrenocorticism
(excessive secretion of ACTH
hormone)
HURLERS SYNDROME
OR GORGOYLISM OR
MPS
Carbohydrate storage
disease
mucopolysacharidosis
HUNTER
SYNDROME
MPS II
WATERHOUSE-
FRIDERICHSEN
SYNDROME
Acute adrenal insufficiency
Acute septicemia

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