| McKusick-Kaufman syndrome: the diagnostic challenge of abdominal distension in the neonatal period. | |
| | |
MedLine Citation:
|
PMID: 1505577 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
|
We report a newborn girl with McKusick-Kaufman syndrome who presented at birth with severe life-threatening abdominal distension due to hydrometrocolpos. In children with polydactyly and cystic masses in the lower abdomen should hydrometrocolpos be especially considered. Ultrasonography is of great value in the correct assignment of lower abdominal tumours, but should be completed by vagino(cysto)scopy when hydrometrocolpos is suspected. |
| | |
Authors:
|
C Schaap; C E de Die-Smulders; R H Kuijten; J P Fryns |
Related Documents
:
|
21494067 - Effectiveness of unilateral pallidotomy for meige syndrome confirmed by motion analysis. 8102637 - Delusional misidentification and dangerousness: a neurobiologic hypothesis. 21556867 - Wallenberg's syndrome with extradural-extracranial origin of the posterior inferior cer... 3968717 - An unusual angiographic appearance of aorto-iliac disease presenting as the leriche syn... 9859107 - Hellp syndrome: undiagnosed in a case of impending rupture of uterus. a case report. 8834257 - Ablepharon macrostomia syndrome with associated cutis laxa: possible localization to 18q. |
Publication Detail:
|
Type: Case Reports; Journal Article |
Journal Detail:
|
Title: European journal of pediatrics Volume: 151 ISSN: 0340-6199 ISO Abbreviation: Eur. J. Pediatr. Publication Date: 1992 Aug |
Date Detail:
|
Created Date: 1992-09-23 Completed Date: 1992-09-23 Revised Date: 2004-11-17 |
Medline Journal Info:
|
Nlm Unique ID: 7603873 Medline TA: Eur J Pediatr Country: GERMANY |
Other Details:
|
Languages: eng Pagination: 583-5 Citation Subset: IM |
Affiliation:
|
Department of Clinical Genetics, Academic Hospital Maastricht, The Netherlands. |
Export Citation:
|
APA/MLA Format Download EndNote Download BibTex |
| MeSH Terms | |
Descriptor/Qualifier:
|
Abnormalities, Multiple* Female Fingers / abnormalities* Heart Defects, Congenital* Humans Infant, Newborn Syndrome Uterus / abnormalities* Vagina / abnormalities* |
| Comments/Corrections | |
Comment In:
|
Eur J Pediatr. 1998 Feb;157(2):170-1
[PMID:
9504798
]
|
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
Previous Document: Atypical Kawasaki disease: an often missed diagnosis.
Next Document: Robinow syndrome in two siblings from consanguineous parents.