Document Detail


3p deletion syndrome.
MedLine Citation:
PMID:  24036645     Owner:  NLM     Status:  In-Data-Review    
Abstract/OtherAbstract:
3p deletion is a rare cytogenetic finding. Here we describe a 3 months old male with congenital malformations. His karyotype revealed 3p deletion 46,XY,del(3)(p25-pter). The child had flexion deformity of wrist and elbow which has never been reported before.
Authors:
Anupam Kaur Rehan Khan; S Khetarpal
Related Documents :
23476665 - Ischemic bilateral opercular syndrome.
10203435 - Crohn's disease and the melkersson-rosenthal syndrome.
22346085 - Premature ovarian aging in primary infertility: triple x syndrome.
7264685 - Space "phobia": a pseudo-agoraphobic syndrome.
3416885 - Disconnection syndrome in a right-handed patient with right hemispheric speech dominance.
21305355 - Gender variability in presentation with alpers' syndrome: a report of eight patients fr...
Publication Detail:
Type:  Journal Article    
Journal Detail:
Title:  Indian pediatrics     Volume:  50     ISSN:  0974-7559     ISO Abbreviation:  Indian Pediatr     Publication Date:  2013 Aug 
Date Detail:
Created Date:  2013-09-16     Completed Date:  -     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  2985062R     Medline TA:  Indian Pediatr     Country:  India    
Other Details:
Languages:  eng     Pagination:  795-6     Citation Subset:  IM    
Affiliation:
Department of Human Genetics, Guru Nanak Dev University; and , *39-C, Circular Road; Amritsar, Punjab, India. Correspondence to: Dr Anupam Kaur, Reader, Human Genetics, Guru Nanak Dev University Amritsar, Punjab 143 005, India. anupamkaur@yahoo.co.in.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:

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


Previous Document:  Atypical hemolytic uremic syndrome with membranoproliferative glomerulonephritis.
Next Document:  Thoracoscopic ligation of thoracic duct for spontaneous chylothorax.