Document Detail


The Moebius sequence--report of a case and a short annotation.
MedLine Citation:
PMID:  1305667     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
A Malay baby with multiple cranial nerve involvement consistent with the Moebius sequence (syndrome) is reported. He also had many non-Central Nervous System (CNS) related defects which include limb reduction defects and the Poland sequence. A short annotation and the spectrum of this disorder are presented. In view of many reported related disorders, Moebius sequence may occur as a part of a broader pattern of malformation.
Authors:
S P Ng; N K Ho
Related Documents :
14527297 - Gene annotation: prediction and testing.
20428317 - Gene-oriented ortholog database: a functional comparison platform for orthologous loci.
19680427 - A parsimony approach to biological pathway reconstruction/inference for genomes and met...
15550167 - Gotcha: a new method for prediction of protein function assessed by the annotation of s...
8970167 - Dna fingerprinting techniques for microorganisms. a proposal for classification and nom...
8457377 - Nucleotide sequence analysis of htlv-i isolated from cerebrospinal fluid of a patient w...
Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  The Journal of the Singapore Paediatric Society     Volume:  34     ISSN:  0037-5683     ISO Abbreviation:  J Singapore Paediatr Soc     Publication Date:  1992  
Date Detail:
Created Date:  1993-07-22     Completed Date:  1993-07-22     Revised Date:  2004-11-17    
Medline Journal Info:
Nlm Unique ID:  7507223     Medline TA:  J Singapore Paediatr Soc     Country:  SINGAPORE    
Other Details:
Languages:  eng     Pagination:  226-9     Citation Subset:  IM    
Affiliation:
Department of Neonatal Medicine I, Kandang Kerbau Hospital, Singapore.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Abnormalities, Multiple*
Cranial Nerve Diseases / congenital*,  diagnosis
Facial Paralysis / congenital
Humans
Infant, Newborn
Male
Syndrome

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


Previous Document:  Anhidrotic ectodermal dysplasia (Christ-Siemens-Touraine syndrome)--a case report and review.
Next Document:  The pressure-dependent nature of the rash in Henoch Schönlein purpura.