| Hallermann-Streiff syndrome with hemihypertrophy. | |
| | |
MedLine Citation:
|
PMID: 20964125 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
|
We report on a five year old girl with Hallermann-Streiff syndrome and hemihypertrophy. Hemihypertrophy does not appear to have ever been associated with Hallermann-Streiff syndrome. |
| | |
Authors:
|
D G Dogan; H Karabiber; M D Erhan; M Garipardic; M Davutoglu; E Guler |
Related Documents
:
|
10854825 - Cyclic cushing's disease associated with primary empty sella. 22582855 - The psychiatric phenotype in triple x syndrome: new hypotheses illustrated in two cases. 2743295 - Osteogenesis imperfecta associated with basilar impression and cerebral atrophy: a case... 20482685 - The hand-foot-syndrome associated with medical tumor therapy - classification and manag... 15859395 - A catastrophic case of skin gangrene. 21418035 - The pluripotential effects of hypolipidemic treatment for polycystic ovary syndrome (pc... |
Publication Detail:
|
Type: Case Reports; Journal Article |
Journal Detail:
|
Title: Genetic counseling (Geneva, Switzerland) Volume: 21 ISSN: 1015-8146 ISO Abbreviation: Genet. Couns. Publication Date: 2010 |
Date Detail:
|
Created Date: 2010-10-22 Completed Date: 2010-11-23 Revised Date: - |
Medline Journal Info:
|
Nlm Unique ID: 9015261 Medline TA: Genet Couns Country: Switzerland |
Other Details:
|
Languages: eng Pagination: 329-33 Citation Subset: IM |
Affiliation:
|
Department of Pediatrics, Inönü University, Turgut Ozal Medical Center, Malatya, Turkey. deryagumus@yahoo.com |
Export Citation:
|
APA/MLA Format Download EndNote Download BibTex |
| MeSH Terms | |
Descriptor/Qualifier:
|
Abnormalities, Multiple
/
diagnosis,
genetics* Cataract / genetics Child, Preschool Female Hallermann's Syndrome / diagnosis, genetics* Humans Hypertrophy / diagnosis, genetics Phenotype |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
Previous Document: A case of otocephaly with anencephaly and meningomyelocele.
Next Document: Primary amenorrhoea in a patient with mosaicism for monosomy X and a derivative X-chromosome.