Prolidase deficiency
Prolidase deficiency: Introduction
Prolidase deficiency: A rare metabolic disorder where an enzyme (prolidase) deficiency impairs the breakdown of certain proteins which causes a harmful buildup in the body. The type and severity of symptoms are variable and may include skin disorders, retarded motor development, impaired cognitive development, frequent infections and skeletal abnormalities.
More detailed information about the symptoms,
causes, and treatments of Prolidase deficiency is available below.
Symptoms of Prolidase deficiency
See full list of 16
symptoms of Prolidase deficiency
Wrongly Diagnosed with Prolidase deficiency?
Prolidase deficiency: Complications
Read more about complications of Prolidase deficiency.
Causes of Prolidase deficiency
Read more about causes of Prolidase deficiency.
Misdiagnosis and Prolidase deficiency
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is a possible misdiagnosis of various conditions, such as multiple sclerosis (see symptoms of...read more »
Read more about Misdiagnosis and Prolidase deficiency
Evidence Based Medicine Research for Prolidase deficiency
Medical research articles related to Prolidase deficiency include:
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Prognosis for Prolidase deficiency
Prognosis for Prolidase deficiency:
variable, depends on level of deficiency
More about prognosis of Prolidase deficiency
Research about Prolidase deficiency
Visit our research pages for current research about Prolidase deficiency treatments.
Statistics for Prolidase deficiency
Prolidase deficiency: Broader Related Topics
Types of Prolidase deficiency
User Interactive Forums
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Definitions of Prolidase deficiency:
Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list Prolidase deficiency as a "rare disease".
Source - Orphanet
Contents for Prolidase deficiency: