Clinical, biochemical and enzymatic studies in type I hyperprolinemia associated with chromosomal abnormality.
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چکیده
منابع مشابه
Clinical, biochemical and enzymatic studies in type I hyperprolinemia associated with chromosomal abnormality.
A severe mentally retarded infant with type I hyperprolinemia associated with chromosomal abnormality is reported. The patient had a characteristic facial appearance of hyperprolinemia and suffered from convulsions after the age of 10 months. The child developed severe mental and motor retardation. The karyotype of the patient revealed partial duplication of the short arm in chromosome 10 using...
متن کاملBiochemical and clinical features of hereditary hyperprolinemia
There are two classifications of hereditary hyperprolinemia: type I (HPI) and type II (HPII). Each type is caused by an autosomal recessive inborn error of the proline metabolic pathway. HPI is caused by an abnormality in the proline-oxidizing enzyme (POX). HPII is caused by a deficiency of Δ-1-pyrroline-5-carboxylate (P5C) dehydrogenase (P5CDh). The clinical features of HPI are unclear. Nephro...
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Background and Objective: Failure to thrive (FTT) is a sign that describes a particular problem rather than a diagnosis and explain growth failure or more advanced failure to gain weight appropriately. The aim of this study was to determine the prevalence and type of chromosomal abnormalities in patients presented with FTT. Materials and Method: One hundred FTT cases with clinical impressio...
متن کاملType I hyperprolinemia: genotype/phenotype correlations.
Type I hyperprolinemia (HPI) is an autosomal recessive disorder associated with cognitive and psychiatric troubles, caused by alterations of the Proline Dehydrogenase gene (PRODH) at 22q11. HPI results from PRODH deletion and/or missense mutations reducing proline oxidase (POX) activity. The goals of this study were first to measure in controls the frequency of PRODH variations described in HPI...
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ژورنال
عنوان ژورنال: The Tohoku Journal of Experimental Medicine
سال: 1987
ISSN: 0040-8727,1349-3329
DOI: 10.1620/tjem.151.465