| Sanjad-Sakati syndrome in a neonate. | |
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MedLine Citation:
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PMID: 20519790 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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Congenital hypoparathyroidism, growth retardation and dysmorphism is a rare autosomal recessive syndrome among Arab population commonly known as Sanjad-Sakati syndrome(SSS).Several metabolic and septic complications are known to manifest in the neonatal age. We describe the first report of morbid pathological fractures affecting a neonate with SSS. |
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Authors:
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Kamalesh Pal |
Publication Detail:
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Type: Case Reports; Journal Article |
Journal Detail:
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Title: Indian pediatrics Volume: 47 ISSN: 0974-7559 ISO Abbreviation: Indian Pediatr Publication Date: 2010 May |
Date Detail:
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Created Date: 2010-06-03 Completed Date: 2010-09-23 Revised Date: 2010-11-15 |
Medline Journal Info:
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Nlm Unique ID: 2985062R Medline TA: Indian Pediatr Country: India |
Other Details:
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Languages: eng Pagination: 443-4 Citation Subset: IM |
Affiliation:
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Department of Pediatric Surgery, Maternity and Childrens Hospital, AI Ahsa. Kingdom of Saudi Arabia. kamalesh_pal@yahoo.com |
Export Citation:
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| MeSH Terms | |
Descriptor/Qualifier:
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Animals Body Dysmorphic Disorders Dietary Supplements Fractures, Bone / pathology, radiography Genetic Diseases, Inborn* / diagnosis, pathology, radiography Humans Humerus / pathology, radiography Hypoparathyroidism Infant, Newborn Male Milk Syndrome Tibia / pathology, radiography |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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