| A male newborn infant with fatco syndrome (fibular aplasia, tibial campomelia and oligodactyly): a case report. | |
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MedLine Citation:
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PMID: 20964118 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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We report a male infant with fibular aplasia, tibial campomelia, and oligosyndactyly (FATCO syndrome). Radiographs showed a short angulated left tibia with fibular aplasia and ipsilateral oligodactyly. We consider our case the 7th patient with FATCO syndrome. |
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Authors:
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A Karaman; H Kahveci |
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Publication Detail:
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Type: Case Reports; Journal Article |
Journal Detail:
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Title: Genetic counseling (Geneva, Switzerland) Volume: 21 ISSN: 1015-8146 ISO Abbreviation: Genet. Couns. Publication Date: 2010 |
Date Detail:
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Created Date: 2010-10-22 Completed Date: 2010-11-23 Revised Date: - |
Medline Journal Info:
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Nlm Unique ID: 9015261 Medline TA: Genet Couns Country: Switzerland |
Other Details:
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Languages: eng Pagination: 285-8 Citation Subset: IM |
Affiliation:
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Department of Medical Genetics, Erzurum Nenehatun Obstetrics and Gynecology Hospital, Erzurum, Turkey. alikaramandr@hotmail.com |
Export Citation:
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| MeSH Terms | |
Descriptor/Qualifier:
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Abnormalities, Multiple
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genetics* Campomelic Dysplasia / genetics* Ectromelia / genetics* Female Fibula / abnormalities* Heterozygote Detection Humans Infant, Newborn Male Phenotype Pregnancy Syndactyly / genetics* Syndrome Tibia / abnormalities* Toes / abnormalities* Ultrasonography, Prenatal |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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