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Prolidase deficiency is a rare autosomal recessive disorder characterized by recurrent and non-healing skin ulcers along with facial dysmorphism and mental retardation. We report a 13-year-old girl who has clinical manifestation of Proliodase deficiency. It is a very rare disorder and no such case has been reported so far from Pakistan.
Dr Arshad Khushdil, Fatima Murtaza. (2017) A CASE OF 13-YEAR-OLD GIRL WITH PROLIDASE DEFICIENCY, JOURNAL OF AYUB MEDICAL COLLEGE ABBOTTABAD, Volume 29, Issue 2.
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