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4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency

4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency: Introduction

4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency: A very rare metabolic disorder where a deficiency of a particular enzyme results in the urinary excretion of a chemical called hawkinsin. Symptoms start once the infant is weaned off breast milk. More detailed information about the symptoms, causes, and treatments of 4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency is available below.

Symptoms of 4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency

Wrongly Diagnosed with 4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency?

4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency: Deaths

Read more about Deaths and 4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency.

4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency: Complications

Read more about complications of 4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency.

Causes of 4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency

Read more about causes of 4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency.

Disease Topics Related To 4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency

Research the causes of these diseases that are similar to, or related to, 4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency:

Misdiagnosis and 4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency

Vitamin B12 deficiency under-diagnosed: The condition of Vitamin B12 deficiency is a possible misdiagnosis of various conditions, such as multiple sclerosis (see symptoms of multiple sclerosis). See symptoms of Vitamin B12...read more »

Statistics for 4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency

4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency: Broader Related Topics

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Definitions of 4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency:

4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that 4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency, or a subtype of 4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Ophanet, a consortium of European partners, currently defines a condition rare when it affects 1 person per 2,000. They list 4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency as a "rare disease".
Source - Orphanet

Related 4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency Info

More information about 4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency

  1. 4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Deaths
  7. Complications
 

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