Document Detail


CHILD syndrome with thrombocytosis and congenital dislocation of hip: A case report from India.
MedLine Citation:
PMID:  20804683     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Congenital Hemidysplasia with Ichthyosiform Nevus and Limb Defects (CHILD) is a very rare entity inherited as an X-linked trait. The cutaneous lesions are characteristic and usually involve the right side of the body. We report a case of CHILD syndrome in an Indian child affecting the left side with various other associations not yet described in the literature, such as thrombocytosis and congenital dislocation of the hip. The rarity of the syndrome prompted us to report this case.
Authors:
Ram Chander; Bincy Varghese; Masarat Jabeen; Taru Garg; Manjula Jain
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Publication Detail:
Type:  Case Reports; Journal Article     Date:  2010-08-15
Journal Detail:
Title:  Dermatology online journal     Volume:  16     ISSN:  1087-2108     ISO Abbreviation:  Dermatol. Online J.     Publication Date:  2010  
Date Detail:
Created Date:  2010-08-31     Completed Date:  2010-12-27     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  9610776     Medline TA:  Dermatol Online J     Country:  United States    
Other Details:
Languages:  eng     Pagination:  6     Citation Subset:  IM    
Affiliation:
Department of Dermatology, Venereology and Leprosy, Lady Hardinge Medical College, New Delhi, India. chanderram41@gmail.com
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MeSH Terms
Descriptor/Qualifier:
Dermatologic Agents / therapeutic use
Emollients / therapeutic use
Female
Hip Dislocation, Congenital / diagnosis*
Humans
Ichthyosiform Erythroderma, Congenital / diagnosis*,  drug therapy,  pathology
India
Infant, Newborn
Limb Deformities, Congenital / diagnosis*
Nevus / diagnosis*,  pathology
Skin Neoplasms / diagnosis*,  pathology
Thrombocytosis / diagnosis*
Treatment Outcome
Chemical
Reg. No./Substance:
0/Dermatologic Agents; 0/Emollients

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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