| Congenital microcephaly and infantile nephrotic syndrome--a case report. | |
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MedLine Citation:
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PMID: 8142231 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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A 22-month-old girl with nephrotic syndrome and microcephaly is described. She had dysmorphic facies and psychomotor retardation. Her parents were first-degree relatives and one of her siblings had died with nephrotic syndrome and renal failure in infancy. An autosomal recessive inheritance is suggested. The diagnosis of this rare combination is discussed and the relevant literature is reviewed. |
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Authors:
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F Yalçinkaya; N Tümer; M Ekim; S Kuyucu; N Cakar; C Ensari |
Publication Detail:
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Type: Case Reports; Journal Article |
Journal Detail:
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Title: Pediatric nephrology (Berlin, Germany) Volume: 8 ISSN: 0931-041X ISO Abbreviation: Pediatr. Nephrol. Publication Date: 1994 Feb |
Date Detail:
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Created Date: 1994-05-04 Completed Date: 1994-05-04 Revised Date: 2004-11-17 |
Medline Journal Info:
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Nlm Unique ID: 8708728 Medline TA: Pediatr Nephrol Country: GERMANY |
Other Details:
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Languages: eng Pagination: 72-3 Citation Subset: IM |
Affiliation:
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Department of Paediatric Nephrology, Ankara University Faculty of Medicine, Turkey. |
Export Citation:
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APA/MLA Format Download EndNote Download BibTex |
| MeSH Terms | |
Descriptor/Qualifier:
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Cyclophosphamide
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therapeutic use Female Humans Infant Microcephaly / complications* Nephrotic Syndrome / complications*, drug therapy Prednisolone / therapeutic use Psychomotor Disorders / complications, genetics |
| Chemical | |
Reg. No./Substance:
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50-18-0/Cyclophosphamide; 50-24-8/Prednisolone |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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