Document Detail


Congenital fusion of the fourth and fifth metacarpals associated with primary gonadal failure.
MedLine Citation:
PMID:  8741065     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Congenital fusion of the fourth and fifth metacarpals is described in a male infant and his maternal grandfather. Primary gonadal failure, which is present in the infant, has not been noted in previously, reported cases. The pedigree in this family is compatible with X-linked recessive or autosomal dominant inheritance with incomplete penetrance.
Authors:
W D Donovan; P W Brill; P Winchester; P F Giampietro; J G Davis; M Harbison
Related Documents :
25307245 - Cesarean deliveries and other risks for persistent pulmonary hypertension of the newborn.
10466615 - A rare case of completely isolated duplication cyst of the alimentary tract.
10797425 - Oeis complex--a population study.
10569405 - Laryngomalacia and its treatment.
7182805 - A possible analogy between contours in mathematics--as exemplified by cauchy's integral...
12499575 - Development of the chymase inhibitor as an anti-tissue-remodeling drug: myocardial infa...
Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  Skeletal radiology     Volume:  25     ISSN:  0364-2348     ISO Abbreviation:  Skeletal Radiol.     Publication Date:  1996 Apr 
Date Detail:
Created Date:  1996-10-24     Completed Date:  1996-10-24     Revised Date:  2004-11-17    
Medline Journal Info:
Nlm Unique ID:  7701953     Medline TA:  Skeletal Radiol     Country:  GERMANY    
Other Details:
Languages:  eng     Pagination:  269-71     Citation Subset:  IM    
Affiliation:
Department of Radiology, New York Hospital-Cornell Medical Center, NY 10021, USA.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Fingers / abnormalities
Genes, Dominant
Genes, Recessive
Hand Deformities, Congenital / complications*,  genetics
Humans
Hypogonadism / complications*
Infant
Linkage (Genetics)
Male
Metacarpus / abnormalities*
Pedigree
X Chromosome

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


Previous Document:  Osseous metaplasia associated with amyloid-producing plasmacytoma of bone: a report of two cases.
Next Document:  Calcific tenosynovitis associated with calcific myonecrosis of the leg: imaging features.