Acromelia‐oligodontia syndrome

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, expandin...

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Detalles Bibliográficos
Autores principales: Talasila, Jyothirmai, Pachigolla, Ramaswamy, Yarlagadda, Kiranmai V. S. N., Vuppala, Ramu, Grzeschik, Karl‐Heinz, Kiran K.V.S, Sai, Rose, Catherine M., Gottesman, Gary S., Urban, Zsolt
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5458011/
https://www.ncbi.nlm.nih.gov/pubmed/28588849
http://dx.doi.org/10.1002/ccr3.956
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author Talasila, Jyothirmai
Pachigolla, Ramaswamy
Yarlagadda, Kiranmai V. S. N.
Vuppala, Ramu
Grzeschik, Karl‐Heinz
Kiran K.V.S, Sai
Rose, Catherine M.
Gottesman, Gary S.
Urban, Zsolt
author_facet Talasila, Jyothirmai
Pachigolla, Ramaswamy
Yarlagadda, Kiranmai V. S. N.
Vuppala, Ramu
Grzeschik, Karl‐Heinz
Kiran K.V.S, Sai
Rose, Catherine M.
Gottesman, Gary S.
Urban, Zsolt
author_sort Talasila, Jyothirmai
collection PubMed
description 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.
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spelling pubmed-54580112017-06-06 Acromelia‐oligodontia syndrome Talasila, Jyothirmai Pachigolla, Ramaswamy Yarlagadda, Kiranmai V. S. N. Vuppala, Ramu Grzeschik, Karl‐Heinz Kiran K.V.S, Sai Rose, Catherine M. Gottesman, Gary S. Urban, Zsolt Clin Case Rep Case Reports 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. John Wiley and Sons Inc. 2017-05-05 /pmc/articles/PMC5458011/ /pubmed/28588849 http://dx.doi.org/10.1002/ccr3.956 Text en © 2017 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Case Reports
Talasila, Jyothirmai
Pachigolla, Ramaswamy
Yarlagadda, Kiranmai V. S. N.
Vuppala, Ramu
Grzeschik, Karl‐Heinz
Kiran K.V.S, Sai
Rose, Catherine M.
Gottesman, Gary S.
Urban, Zsolt
Acromelia‐oligodontia syndrome
title Acromelia‐oligodontia syndrome
title_full Acromelia‐oligodontia syndrome
title_fullStr Acromelia‐oligodontia syndrome
title_full_unstemmed Acromelia‐oligodontia syndrome
title_short Acromelia‐oligodontia syndrome
title_sort acromelia‐oligodontia syndrome
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5458011/
https://www.ncbi.nlm.nih.gov/pubmed/28588849
http://dx.doi.org/10.1002/ccr3.956
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AT rosecatherinem acromeliaoligodontiasyndrome
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