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www.healthdigeZt.com
AS RECEIVED :
DR. TONY ALMEIDA
( Bombay Kidney Speciality expert )
made the extensive experiments with
perseverance and patience and
discovered a successful treatment for
diabetes.
Now a days a lot of people, old men &
women in particular suffer a lot due to
Diabetes.
Ingredients:
1 - Wheat 100 gm
2 - Gum(of tree) (gondh) 100 gm
3 - Barley 100 gm
4 - Black Seeds (kalunji) 100 gm
A woman (65) was diabetic for the
last 20+ years
and was taking insulin twice
a day.
She used the enclosed
homemade medicine for a
fortnight and
now she is absolutely free of
diabetes and taking all her
food as normal including
sweets.
The doctors have advised
her to stop insulin and any
other blood sugar controlling
drugs.
I request you all please
circulate the email below to
as many people as you can
and let them take maximum
benefit from it.
Method of Preparation :
Put all the above ingredients in 5 cups of water.
Boil it for 10 minutes and put off the fire.
Allow it to cool down by itself.
When it has become cold, filter out the
seeds and preserve water in a glass jug or bottle.
How to use it?
Take one small cup of this water every day early morning when your stomach is empty.
Continue this for 7 days.
Next week repeat the same but on alternate days. With these 2 weeks of
treatment you will wonder to see that you have become normal and can eat
normal food without problem.
Note:
A request is to spread this to as many as possible so that others can
also take benefit out of it.
SINCE THESE ARE ALL NATURAL INGREDIENTS,
TAKING THEM IS NOT HARMFUL.
SO THOSE WHO ARE SCEPTICAL ABOUT THIS TREATMENT
MAY STILL TRY IT WITHOUT ANY HARM.
•
METABOLIC DISORDERS OF
AMINOACIDS
,PROTIENS,CARBOHYDRATES
AND LIPIDS
METABOLIC DISORDER
OF PROTIENS AND
AMINO ACIDS
METABOLIC DISORDERS OF
AMINOACIDS
•UREA
•PHENYL ALANINE AND TYROSINE
•SULPHUR AMINO ACIDS
•GLYCINE
•TROPTOPHAN
•BRANCHED CHAIN AMINO ACIDS
•HISTIDINE
•PROLINE
ENZYME INVOLVED DEFECTS
CARBAMONYL PHOSPHATE
SYNTHASE-I
HYPERAMMONEMIA
TYPE-I
ORNITHINE
TRANSCARBAMOLYSE
HYPERAMMONEMIA
TYPE-II
AGGINOSUCCINATE
SYNTHASE
CITRULLINEMIA
ARGINOSUCCINASE ARGINOSUCCINIC ACID
. Phenylalanine AND tyrosine
ENZYME DISORDER
Pehenylalanin
hydroxylase
. Phenylketonuria
Tyrosine transaminase Tyrosinema type -
II
P-hydroxy phenylpyruvate
dioxygenase
Neonatal
tyrosinema
Hiomogenisate oxidase alkaptonuria
Maleyl acetoacetate
isomerase
tyrosinosis
tyrosinase albinism
SULPHUR AMINO ACIDS
(methionine,cystine,cysteine)
Enzyme/metabolic effect disorder
Deffect in renal absorption cystinuria
Impairment in cystine
utilization
cystinosis
Cystathionine synthetase Homacystinuria type I
N5,N10-METHYLENE THF
REDUCTASE
Homo cystinuria type -II
N5-methyl THF –
homocysteine
methyltranferase
Homocystinuria-III
GLYCINE
METABOLIC
DEFFECT/ENZYME
DISORDER
DEFECT IN RENAL
REABSORPTION
GLYCINURIA
GLYCINE TRANS
AMINASE
PRIMART
HYPEROXALURIA
BRANCHED AMINO ACIDS
(VALINE,LEUCINE,ISOLUECINE)
METABOLIC
DEFFECT/ENZYME
DISORDER
BRANCHED CHAIN
HALPHA-KETO
ACID
DEHYDROGENASE
MAPLE SYRUP
URINE DISEASE
VARIANT OF ABOVE
ENZYMES
INTRMITTENT
BRANCHED CHAIN
KETO NEURIA
VALINE TRANS
AMINASE
HYPERVALINEMIA
ISOVALERYL CO-A
DEHYDROGENASE
ISOVALERIC
ACIDEMIA
TRYPTOPHAN
HISTIDINE
PROLINE
METABOLIC
EFFECT
DISORDER
DEFECTIVE
INTESTINAL
ABSORPTION
HARTUP’S DISEASE
ENZYME DISORDER
HISTIDASE HISTIDINEMIA
ENZYME DISORDER
PROLINE OXIDASE HYPERPROLINEMIA
TYPE-I
METABOLIC
DISORDERS
CARBOHYDRATES
Name of disease Enzyme defect
VON GIERKE’S DISEASE GLUCOSE PHOSPAHA
POMPR’S DISEASE LYSOSOMAL HALPHA-1,4-
GLUCOSIDASE
ANDERSON’S DISEASE GLUCOSYL-4-6-TRANSFERASE
McARDLE’S DISEASE MUSCLE GLYCOGEN
PHOSPHORYLASE
HER’S DISEASE LIVER GLYCOGEN
PHOSPHORYLASE
TARUI’S DISEASE PHOPHOFRUCTOKINASE
COR’S DISEASE GLYCOSYL TRANSFERASE
DURING HMP AND GLYCOLYSIS
ENZYME/METABOLIC DEFFECT DISORDER
PYRUVATE DEHDOGRNASE ACCUMILATION OF
PYRUVATE,LACTIC
ACIDOSIS
PYRUVATE KINASE AND ALDOLASE-
A
HEMOLYTIC ANEMIA
MUSCLE PHOSPHO FRUCTOKINASE LOW EXERCISE CAPACITY
GLUCOSE-6-
PHOSPHATEDEHYDROGENASE
HEMOLYTIC ANEMIA
EXCESS UPTAKE OF FRUCTOSE HYPERURICEMIA/GOUT
HEPATIC FRUCTOKINASE FRUCTOSURIA
FRUCTOSE-1,6-BISPHOSPHATAE GALACTOSEMIAS
TRANSKETOLASE WERNICKE KORSAKOFF
SYNDROME
METABOLIC DISORDERS
OF LIPIDS
METABOLIC
EFFECT/ENZYME
DISORDER
ACEYL CO-A
DEHYDRGENASE
INFANT DEATH
SYNDROME
METHYL MALONYL CO-A
MUTASE
METHYL MALONIC
ACIDEMIA
INCRESE CHOLESTROL DIABETES MELLITUS
DECREASE HDL HYPOTHYRODISM
OBSTRUCTION OF
CHOLESTROL
EXCRESTION
OBSTRUCTIVE JAUNDICE
CARNITINE DEFICENCY HYPOGLYCEMIA
KETOGENESIS NONKETOTIC
METABOLIC EFFECT/ENZYME DISORDER
3-KETOACYL-COA THIOLASE
AND HMG-CO-A LYASE
DEGRADATION OF LEUCINE
ACYL CO-A DEHYDROGENASE JAMAICAN VOMITTING
SICKNESS AND DICARBOXYLIC
ACIDUREA
LACK OF PHYTANIC ACID REFSUM’S DISEASE
ABESENC OF PEROXISOMES
IN TISSUES AND ELIVATED
LEVELS OF POLYENOIC ACIDS
ZELLWER’S SYNDROME
(CEREBROHEPTORENAL)
EXCESS KETONE BODIES KETOSIS
PROLONS KETOSIS KETOACIDS
ACCUMULATION OF CORANARY HEART DISEASES
REFERENCE
U.SATYANARAYANA
HARPER’S
MADE BY
YOSHASRI.J
NISHITHA.V

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Metabolic disorders

  • 1. www.healthdigeZt.com AS RECEIVED : DR. TONY ALMEIDA ( Bombay Kidney Speciality expert ) made the extensive experiments with perseverance and patience and discovered a successful treatment for diabetes. Now a days a lot of people, old men & women in particular suffer a lot due to Diabetes. Ingredients: 1 - Wheat 100 gm 2 - Gum(of tree) (gondh) 100 gm 3 - Barley 100 gm 4 - Black Seeds (kalunji) 100 gm A woman (65) was diabetic for the last 20+ years and was taking insulin twice a day. She used the enclosed homemade medicine for a fortnight and now she is absolutely free of diabetes and taking all her food as normal including sweets. The doctors have advised her to stop insulin and any other blood sugar controlling drugs. I request you all please circulate the email below to as many people as you can and let them take maximum benefit from it.
  • 2. Method of Preparation : Put all the above ingredients in 5 cups of water. Boil it for 10 minutes and put off the fire. Allow it to cool down by itself. When it has become cold, filter out the seeds and preserve water in a glass jug or bottle. How to use it? Take one small cup of this water every day early morning when your stomach is empty. Continue this for 7 days. Next week repeat the same but on alternate days. With these 2 weeks of treatment you will wonder to see that you have become normal and can eat normal food without problem. Note: A request is to spread this to as many as possible so that others can also take benefit out of it. SINCE THESE ARE ALL NATURAL INGREDIENTS, TAKING THEM IS NOT HARMFUL. SO THOSE WHO ARE SCEPTICAL ABOUT THIS TREATMENT MAY STILL TRY IT WITHOUT ANY HARM. •
  • 5. METABOLIC DISORDERS OF AMINOACIDS •UREA •PHENYL ALANINE AND TYROSINE •SULPHUR AMINO ACIDS •GLYCINE •TROPTOPHAN •BRANCHED CHAIN AMINO ACIDS •HISTIDINE •PROLINE
  • 6. ENZYME INVOLVED DEFECTS CARBAMONYL PHOSPHATE SYNTHASE-I HYPERAMMONEMIA TYPE-I ORNITHINE TRANSCARBAMOLYSE HYPERAMMONEMIA TYPE-II AGGINOSUCCINATE SYNTHASE CITRULLINEMIA ARGINOSUCCINASE ARGINOSUCCINIC ACID
  • 7. . Phenylalanine AND tyrosine ENZYME DISORDER Pehenylalanin hydroxylase . Phenylketonuria Tyrosine transaminase Tyrosinema type - II P-hydroxy phenylpyruvate dioxygenase Neonatal tyrosinema Hiomogenisate oxidase alkaptonuria Maleyl acetoacetate isomerase tyrosinosis tyrosinase albinism
  • 8. SULPHUR AMINO ACIDS (methionine,cystine,cysteine) Enzyme/metabolic effect disorder Deffect in renal absorption cystinuria Impairment in cystine utilization cystinosis Cystathionine synthetase Homacystinuria type I N5,N10-METHYLENE THF REDUCTASE Homo cystinuria type -II N5-methyl THF – homocysteine methyltranferase Homocystinuria-III
  • 10. BRANCHED AMINO ACIDS (VALINE,LEUCINE,ISOLUECINE) METABOLIC DEFFECT/ENZYME DISORDER BRANCHED CHAIN HALPHA-KETO ACID DEHYDROGENASE MAPLE SYRUP URINE DISEASE VARIANT OF ABOVE ENZYMES INTRMITTENT BRANCHED CHAIN KETO NEURIA VALINE TRANS AMINASE HYPERVALINEMIA ISOVALERYL CO-A DEHYDROGENASE ISOVALERIC ACIDEMIA
  • 13. Name of disease Enzyme defect VON GIERKE’S DISEASE GLUCOSE PHOSPAHA POMPR’S DISEASE LYSOSOMAL HALPHA-1,4- GLUCOSIDASE ANDERSON’S DISEASE GLUCOSYL-4-6-TRANSFERASE McARDLE’S DISEASE MUSCLE GLYCOGEN PHOSPHORYLASE HER’S DISEASE LIVER GLYCOGEN PHOSPHORYLASE TARUI’S DISEASE PHOPHOFRUCTOKINASE COR’S DISEASE GLYCOSYL TRANSFERASE
  • 14. DURING HMP AND GLYCOLYSIS ENZYME/METABOLIC DEFFECT DISORDER PYRUVATE DEHDOGRNASE ACCUMILATION OF PYRUVATE,LACTIC ACIDOSIS PYRUVATE KINASE AND ALDOLASE- A HEMOLYTIC ANEMIA MUSCLE PHOSPHO FRUCTOKINASE LOW EXERCISE CAPACITY GLUCOSE-6- PHOSPHATEDEHYDROGENASE HEMOLYTIC ANEMIA EXCESS UPTAKE OF FRUCTOSE HYPERURICEMIA/GOUT HEPATIC FRUCTOKINASE FRUCTOSURIA FRUCTOSE-1,6-BISPHOSPHATAE GALACTOSEMIAS TRANSKETOLASE WERNICKE KORSAKOFF SYNDROME
  • 16. METABOLIC EFFECT/ENZYME DISORDER ACEYL CO-A DEHYDRGENASE INFANT DEATH SYNDROME METHYL MALONYL CO-A MUTASE METHYL MALONIC ACIDEMIA INCRESE CHOLESTROL DIABETES MELLITUS DECREASE HDL HYPOTHYRODISM OBSTRUCTION OF CHOLESTROL EXCRESTION OBSTRUCTIVE JAUNDICE CARNITINE DEFICENCY HYPOGLYCEMIA KETOGENESIS NONKETOTIC
  • 17. METABOLIC EFFECT/ENZYME DISORDER 3-KETOACYL-COA THIOLASE AND HMG-CO-A LYASE DEGRADATION OF LEUCINE ACYL CO-A DEHYDROGENASE JAMAICAN VOMITTING SICKNESS AND DICARBOXYLIC ACIDUREA LACK OF PHYTANIC ACID REFSUM’S DISEASE ABESENC OF PEROXISOMES IN TISSUES AND ELIVATED LEVELS OF POLYENOIC ACIDS ZELLWER’S SYNDROME (CEREBROHEPTORENAL) EXCESS KETONE BODIES KETOSIS PROLONS KETOSIS KETOACIDS ACCUMULATION OF CORANARY HEART DISEASES