Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Jain, Puneet, Sharma, Suvasini, Kumar, Atin, Aneja, Satinder
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
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
_version_ 1782318536266350592
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
work_keys_str_mv AT jainpuneet pontocerebellarhypoplasiatype1withamilderphenotypeinatwoyearoldgirl
AT sharmasuvasini pontocerebellarhypoplasiatype1withamilderphenotypeinatwoyearoldgirl
AT kumaratin pontocerebellarhypoplasiatype1withamilderphenotypeinatwoyearoldgirl
AT anejasatinder pontocerebellarhypoplasiatype1withamilderphenotypeinatwoyearoldgirl