Document Detail


Cutis marmorata telangiectatica with multiple congenital anomalies (van Lohuizen's syndrome).
MedLine Citation:
PMID:  7333396     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
A 5-year-old Korean boy with diagnosis of cutis marmorata telangiectatica congenita had a bluish-red, widespread livedo network over the entire body surface. There was skin atrophy as well as ulceration and crust over some of the lesions. These abnormalities have been associated with mental retardation with abnormal EEG findings, speech disability, defective growth, cleft palate, presence of simian lines and an increase in the atd angles of both palms, diffuse demineralization of bony structure and weakness of the long extensor muscles of both thumbs. Based on our clinical datas and review of world literature, it would seem to be necessary to change the terminology.
Authors:
S Lee; J B Lee; J H Kim; K Y Kim; S H Lee
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Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  Dermatologica     Volume:  163     ISSN:  0011-9075     ISO Abbreviation:  Dermatologica     Publication Date:  1981  
Date Detail:
Created Date:  1982-05-27     Completed Date:  1982-05-27     Revised Date:  2004-11-17    
Medline Journal Info:
Nlm Unique ID:  0211607     Medline TA:  Dermatologica     Country:  SWITZERLAND    
Other Details:
Languages:  eng     Pagination:  408-12     Citation Subset:  IM    
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MeSH Terms
Descriptor/Qualifier:
Abnormalities, Multiple / pathology*
Child, Preschool
Humans
Male
Skin Diseases / complications,  congenital*,  pathology
Syndrome
Telangiectasis / pathology
Vasculitis / complications,  pathology*

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


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