Document Detail


Bilateral cryptorchidism associated with terminal deletion of 10q.
MedLine Citation:
PMID:  9933844     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
We report on an infant with terminal deletion of 10q (del10q26.11) presenting with bilateral cryptorchidism. Of 9 males previously reported with terminal deletion of 10q, 1 had an intersex phenotype, and the others all had combinations of cryptorchidism, micropenis, and hypospadias. Terminal deletion of 10q appears to include some genes indispensable for normal male genital development.
Authors:
Y Suzuki; I Sasagawa; T Nakada; Y Onmura
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Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  Urologia internationalis     Volume:  61     ISSN:  0042-1138     ISO Abbreviation:  Urol. Int.     Publication Date:  1998  
Date Detail:
Created Date:  1999-03-23     Completed Date:  1999-03-23     Revised Date:  2006-10-30    
Medline Journal Info:
Nlm Unique ID:  0417373     Medline TA:  Urol Int     Country:  SWITZERLAND    
Other Details:
Languages:  eng     Pagination:  186-7     Citation Subset:  IM    
Affiliation:
Department of Urology, Yamagata University School of Medicine, Yamagata, Japan.
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MeSH Terms
Descriptor/Qualifier:
Chromosome Deletion*
Chromosomes, Human, Pair 10*
Cryptorchidism / genetics*,  pathology
Humans
Infant
Male
Sex Differentiation / genetics*

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


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