| Severe form of hypoglossia-hypodactylia syndrome associated with complex cardiopathy: a case report. | |
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MedLine Citation:
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PMID: 20637513 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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Hypoglossia is a rare congenital anomaly and is frequently associated with limb anomalies. In 1971, Hall employed the term hypoglossia-hypodactylia syndrome for the classification of these oromandibular-limb hypogenesis syndromes. The syndrome is characterized by hypoglossia, micrognathia mandible and variable degrees of limb abnormalities, frequent gingival abnormalities, and an absence of mandibular incisors. We describe an unusual case of hypoglossia-hypodactylia syndrome. The newborn had hypoglossia, limb defects and complex congenital cardiopathy, which has to date never been reported to be associated to this syndrome. |
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Authors:
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Siham Chafai Elalaoui; Ilham Ratbi; Mohamed Malih; Mohamed Bounasse; Abdelaziz Sefiani |
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Publication Detail:
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Type: Case Reports; Journal Article Date: 2010-07-15 |
Journal Detail:
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Title: International journal of pediatric otorhinolaryngology Volume: 74 ISSN: 1872-8464 ISO Abbreviation: Int. J. Pediatr. Otorhinolaryngol. Publication Date: 2010 Sep |
Date Detail:
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Created Date: 2010-08-16 Completed Date: 2010-12-22 Revised Date: - |
Medline Journal Info:
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Nlm Unique ID: 8003603 Medline TA: Int J Pediatr Otorhinolaryngol Country: Ireland |
Other Details:
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Languages: eng Pagination: 1092-4 Citation Subset: IM |
Copyright Information:
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Copyright 2010 Elsevier Ireland Ltd. All rights reserved. |
Affiliation:
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Department of Medical Genetics, National Institute of Health, Rabat, Morocco. |
Export Citation:
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| MeSH Terms | |
Descriptor/Qualifier:
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Abnormalities, Multiple* Female Fingers / abnormalities* Heart Defects, Congenital* Humans Infant, Newborn Mouth Abnormalities Syndrome Tongue / abnormalities* |
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