Document Detail


Sanjad-Sakati syndrome in a neonate.
MedLine Citation:
PMID:  20519790     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
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.
Authors:
Kamalesh Pal
Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  Indian pediatrics     Volume:  47     ISSN:  0974-7559     ISO Abbreviation:  Indian Pediatr     Publication Date:  2010 May 
Date Detail:
Created Date:  2010-06-03     Completed Date:  2010-09-23     Revised Date:  2010-11-15    
Medline Journal Info:
Nlm Unique ID:  2985062R     Medline TA:  Indian Pediatr     Country:  India    
Other Details:
Languages:  eng     Pagination:  443-4     Citation Subset:  IM    
Affiliation:
Department of Pediatric Surgery, Maternity and Childrens Hospital, AI Ahsa. Kingdom of Saudi Arabia. kamalesh_pal@yahoo.com
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MeSH Terms
Descriptor/Qualifier:
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

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