Phenylketonuric embryopathy

Introduction: Phenylketonuric embryopathy

Description of Phenylketonuric embryopathy

Phenylketonuric embryopathy (medical condition): A rare disorder where a mother suffering from phenylketonuria...more »

See also:

Maternal hyperphenylalaninemia:
  »Introduction: Maternal hyperphenylalaninemia
  »Symptoms of Maternal hyperphenylalaninemia

Phenylketonuric embryopathy: Related Topics

These medical condition or symptom topics may be relevant to medical information for Phenylketonuric embryopathy:

• Embryopathy

Phenylketonuric embryopathy: Rare Disease

Ophanet

Ophanet, a consortium of European partners, currently defines a condition rare when if affects 1 person per 2,000. They list Phenylketonuric embryopathy as a "rare disease".

Source - Orphanet

Phenylketonuric embryopathy as a Disease

Phenylketonuric embryopathy: Another name for Maternal hyperphenylalaninemia (or close medical condition association).
  »Introduction: Maternal hyperphenylalaninemia
  »Symptoms of Maternal hyperphenylalaninemia

Phenylketonuric embryopathy: Related Diseases

Phenylketonuric embryopathy: Phenylketonuric embryopathy is listed as a type of (or associated with) the following medical conditions in our database:

• Blood conditions
• Metabolic conditions
• Fetal health conditions
• Pregnancy-related conditions
• Women's health conditions
• Women-only conditions

Symptoms of Phenylketonuric embryopathy (Maternal hyperphenylalaninemia)

Some of the symptoms of Phenylketonuric embryopathy incude:

• Mental deficiency
• Low I Q
• Increased muscle tone
• Pigeon-toed gait
• Growth deficiency

See full list of 19 symptoms of Phenylketonuric embryopathy (Maternal hyperphenylalaninemia)

Phenylketonuric embryopathy: Related Disease Topics

These medical disease topics may be related to Phenylketonuric embryopathy:

• phenylketonuria

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Medical dictionaries:

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• Medical Acronymns/Abbreviations

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