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Dysmorphic Short Stature: Radiological Diagnosis of Trichorhinophalangeal Syndrome

Trichorhinophalangeal syndrome (TRPS), a type of skeletal dysplasia, is characterized by a triad of dysmorphic (bulbous nose and large ears); ectodermal (thin and sparse hair); and skeletal (short stature and cone-shaped epiphyses) findings, and this combination is helpful for early diagnosis and ap...

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Autores principales: Nicolescu, Corina Ramona, Kasongo, Laura, Rausin, Léon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6280227/
https://www.ncbi.nlm.nih.gov/pubmed/30584486
http://dx.doi.org/10.1155/2018/5189062
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author Nicolescu, Corina Ramona
Kasongo, Laura
Rausin, Léon
author_facet Nicolescu, Corina Ramona
Kasongo, Laura
Rausin, Léon
author_sort Nicolescu, Corina Ramona
collection PubMed
description Trichorhinophalangeal syndrome (TRPS), a type of skeletal dysplasia, is characterized by a triad of dysmorphic (bulbous nose and large ears); ectodermal (thin and sparse hair); and skeletal (short stature and cone-shaped epiphyses) findings, and this combination is helpful for early diagnosis and appropriate follow-up. A 14-year-old boy presented with short stature and distinctive facial features, and following the first clinical and biological evaluation, no precise diagnosis was reached. Progressive bilateral development of noninflammatory and painless deformity of his second finger required a radiological exam that highlighted the key elements (cone-shaped epiphyses) for final diagnosis. This case illustrates the difficulties to early recognition of TRPS when the clinical presentation is not complete and radiological findings are missing.
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spelling pubmed-62802272018-12-24 Dysmorphic Short Stature: Radiological Diagnosis of Trichorhinophalangeal Syndrome Nicolescu, Corina Ramona Kasongo, Laura Rausin, Léon Case Rep Pediatr Case Report Trichorhinophalangeal syndrome (TRPS), a type of skeletal dysplasia, is characterized by a triad of dysmorphic (bulbous nose and large ears); ectodermal (thin and sparse hair); and skeletal (short stature and cone-shaped epiphyses) findings, and this combination is helpful for early diagnosis and appropriate follow-up. A 14-year-old boy presented with short stature and distinctive facial features, and following the first clinical and biological evaluation, no precise diagnosis was reached. Progressive bilateral development of noninflammatory and painless deformity of his second finger required a radiological exam that highlighted the key elements (cone-shaped epiphyses) for final diagnosis. This case illustrates the difficulties to early recognition of TRPS when the clinical presentation is not complete and radiological findings are missing. Hindawi 2018-11-21 /pmc/articles/PMC6280227/ /pubmed/30584486 http://dx.doi.org/10.1155/2018/5189062 Text en Copyright © 2018 Corina Ramona Nicolescu et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Nicolescu, Corina Ramona
Kasongo, Laura
Rausin, Léon
Dysmorphic Short Stature: Radiological Diagnosis of Trichorhinophalangeal Syndrome
title Dysmorphic Short Stature: Radiological Diagnosis of Trichorhinophalangeal Syndrome
title_full Dysmorphic Short Stature: Radiological Diagnosis of Trichorhinophalangeal Syndrome
title_fullStr Dysmorphic Short Stature: Radiological Diagnosis of Trichorhinophalangeal Syndrome
title_full_unstemmed Dysmorphic Short Stature: Radiological Diagnosis of Trichorhinophalangeal Syndrome
title_short Dysmorphic Short Stature: Radiological Diagnosis of Trichorhinophalangeal Syndrome
title_sort dysmorphic short stature: radiological diagnosis of trichorhinophalangeal syndrome
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6280227/
https://www.ncbi.nlm.nih.gov/pubmed/30584486
http://dx.doi.org/10.1155/2018/5189062
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