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Pontocerebellar hypoplasia type 1 with a milder phenotype in a two-year-old girl
The rare association of pontocerebellar hypoplasia with anterior horn cell involvement has been classified as pontocerebellar hypoplasia type 1. Its classic phenotype is usually severe. However, the pontocerebellar hypoplasia type 1 may have wider variability in clinical and radiological features. T...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4040042/ https://www.ncbi.nlm.nih.gov/pubmed/24891912 http://dx.doi.org/10.4103/1817-1745.131494 |
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author | Jain, Puneet Sharma, Suvasini Kumar, Atin Aneja, Satinder |
author_facet | Jain, Puneet Sharma, Suvasini Kumar, Atin Aneja, Satinder |
author_sort | Jain, Puneet |
collection | PubMed |
description | The rare association of pontocerebellar hypoplasia with anterior horn cell involvement has been classified as pontocerebellar hypoplasia type 1. Its classic phenotype is usually severe. However, the pontocerebellar hypoplasia type 1 may have wider variability in clinical and radiological features. There may be a genetic heterogeneity as well. We described here a young girl with relatively milder clinical phenotype with cerebellar atrophy with absent pontine involvement, further adding to the clinical phenotype. |
format | Online Article Text |
id | pubmed-4040042 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-40400422014-06-02 Pontocerebellar hypoplasia type 1 with a milder phenotype in a two-year-old girl Jain, Puneet Sharma, Suvasini Kumar, Atin Aneja, Satinder J Pediatr Neurosci Case Report The rare association of pontocerebellar hypoplasia with anterior horn cell involvement has been classified as pontocerebellar hypoplasia type 1. Its classic phenotype is usually severe. However, the pontocerebellar hypoplasia type 1 may have wider variability in clinical and radiological features. There may be a genetic heterogeneity as well. We described here a young girl with relatively milder clinical phenotype with cerebellar atrophy with absent pontine involvement, further adding to the clinical phenotype. Medknow Publications & Media Pvt Ltd 2014 /pmc/articles/PMC4040042/ /pubmed/24891912 http://dx.doi.org/10.4103/1817-1745.131494 Text en Copyright: © Journal of Pediatric Neurosciences http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Jain, Puneet Sharma, Suvasini Kumar, Atin Aneja, Satinder Pontocerebellar hypoplasia type 1 with a milder phenotype in a two-year-old girl |
title | Pontocerebellar hypoplasia type 1 with a milder phenotype in a two-year-old girl |
title_full | Pontocerebellar hypoplasia type 1 with a milder phenotype in a two-year-old girl |
title_fullStr | Pontocerebellar hypoplasia type 1 with a milder phenotype in a two-year-old girl |
title_full_unstemmed | Pontocerebellar hypoplasia type 1 with a milder phenotype in a two-year-old girl |
title_short | Pontocerebellar hypoplasia type 1 with a milder phenotype in a two-year-old girl |
title_sort | pontocerebellar hypoplasia type 1 with a milder phenotype in a two-year-old girl |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4040042/ https://www.ncbi.nlm.nih.gov/pubmed/24891912 http://dx.doi.org/10.4103/1817-1745.131494 |
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