| Hemifacial microsomia in a patient with Klinefelter syndrome. | |
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MedLine Citation:
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PMID: 6930993 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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A patient with 47, XXY karyotype, Klinefelter Syndrome, and hemifacial microsomia (unilateral microtia and mandibular hypoplasia) is described. In view of the fact that this is the second reported patient with hemifacial microsomia and a sex chromosomal abnormality, the relationship of these two findings is discussed. Appropriate diagnostic work-up of the patient with hemifacial microsomia is reviewed. |
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Authors:
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H H Poonawalla; C I Kaye; I M Rosenthal; S Pruzansky |
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Publication Detail:
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Type: Case Reports; Journal Article; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, U.S. Gov't, P.H.S. |
Journal Detail:
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Title: The Cleft palate journal Volume: 17 ISSN: 0009-8701 ISO Abbreviation: Cleft Palate J Publication Date: 1980 Jul |
Date Detail:
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Created Date: 1980-10-24 Completed Date: 1980-10-24 Revised Date: 2006-11-15 |
Medline Journal Info:
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Nlm Unique ID: 0372737 Medline TA: Cleft Palate J Country: UNITED STATES |
Other Details:
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Languages: eng Pagination: 194-6 Citation Subset: D; IM |
Export Citation:
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APA/MLA Format Download EndNote Download BibTex |
| MeSH Terms | |
Descriptor/Qualifier:
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Adolescent Adult Child Ear, External / abnormalities Facial Asymmetry / etiology* Follow-Up Studies Humans Karyotyping Klinefelter Syndrome / complications*, genetics Male Mandible / abnormalities* |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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