Acromelia‐oligodontia syndrome
Identifieur interne : 007025 ( Ncbi/Curation ); précédent : 007024; suivant : 007026Acromelia‐oligodontia syndrome
Auteurs : Jyothirmai Talasila ; Ramaswamy Pachigolla ; Kiranmai V. S. N. Yarlagadda ; Ramu Vuppala ; Karl-Heinz Grzeschik ; Sai Kiran K. V. S ; Catherine M. Rose ; Gary S. Gottesman ; Zsolt UrbanSource :
- Clinical Case Reports [ 2050-0904 ] ; 2017.
Abstract
This case report describes a patient with ankyloglossia, oligodontia, unilateral hypoplasia of the zygoma and mandible, along with bilateral distal reduction anomalies of his limbs without long bone abnormalities. This may represent a mild variant of oromandibular limb hypogenesis syndrome, expanding the phenotypic spectrum, or a previously unrecognized malformation syndrome.
Url:
DOI: 10.1002/ccr3.956
PubMed: 28588849
PubMed Central: 5458011
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PMC:5458011Le document en format XML
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<front><div type="abstract" xml:lang="en"><title>Key Clinical Message</title>
<p>This case report describes a patient with ankyloglossia, oligodontia, unilateral hypoplasia of the zygoma and mandible, along with bilateral distal reduction anomalies of his limbs without long bone abnormalities. This may represent a mild variant of oromandibular limb hypogenesis syndrome, expanding the phenotypic spectrum, or a previously unrecognized malformation syndrome.</p>
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