| Hypertrichosis terminalis, gingival hyperplasia, and a characteristic face: a new distinct entity. | |
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MedLine Citation:
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PMID: 12503107 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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Congenital generalized hypertrichosis terminalis has been described in association with other features as gingival hyperplasia, osteochondrodysplasia, and a dysmorphic face. Bondeson and Miles [1993: Am J Med Genet 47:198-212] described a woman with universal congenital hypertrichosis terminalis associated with gingival hyperplasia; the face of this patient was coarse and different from other forms of hypertrichosis described before. We present an 11-year, 6-month-old girl with universal congenital hypertrichosis terminalis, gingival hyperplasia, and a characteristic coarse face resembling the patient described by Bondeson and Miles [1993: Am J Med Genet 47:198-212]. We propose that this type of congenital generalized hypertrichosis terminalis, associated with gingival hyperplasia and a coarse face, is a distinctive new entity. |
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Authors:
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Sonia Canún; E G Guevara-Sanginés; A Elvira-Morales; Ma del C Sierra-Romero; H Rodríguez-Asbun |
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Publication Detail:
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Type: Case Reports; Journal Article; Review |
Journal Detail:
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Title: American journal of medical genetics. Part A Volume: 116A ISSN: 1552-4825 ISO Abbreviation: Am. J. Med. Genet. A Publication Date: 2003 Jan |
Date Detail:
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Created Date: 2002-12-27 Completed Date: 2003-04-30 Revised Date: 2008-05-21 |
Medline Journal Info:
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Nlm Unique ID: 101235741 Medline TA: Am J Med Genet A Country: United States |
Other Details:
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Languages: eng Pagination: 278-83 Citation Subset: IM |
Copyright Information:
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Copyright 2002 Wiley-Liss, Inc. |
Affiliation:
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División de Genética, Hospital General Dr. Manuel Gea González, México City, México. scanuns@hotmail.com |
| Data Bank Information | |
Bank Name/Acc. No.:
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OMIM/135400; 145700; 145701; 307150 |
Export Citation:
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| MeSH Terms | |
Descriptor/Qualifier:
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Abnormalities, Multiple
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genetics,
pathology* Child Face / abnormalities* Female Gingival Hyperplasia / pathology* Humans Hypertrichosis / pathology* Infant Karyotyping |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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