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Clinical spectrum of woolly hair: indications for cerebral involvement
BACKGROUND: Woolly Hair is an uncommon congenital anomaly of the scalp hair presenting with strongly coiled hair involving a localized area of the scalp or covering the entire side and occurring in non-black people. Isolated or localized wooly hair is usually benign and is not related to other disor...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5667512/ https://www.ncbi.nlm.nih.gov/pubmed/29096685 http://dx.doi.org/10.1186/s13052-017-0417-1 |
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author | Pavone, Piero Falsaperla, Raffaele Barbagallo, Massimo Polizzi, Agata Praticò, Andrea D. Ruggieri, Martino |
author_facet | Pavone, Piero Falsaperla, Raffaele Barbagallo, Massimo Polizzi, Agata Praticò, Andrea D. Ruggieri, Martino |
author_sort | Pavone, Piero |
collection | PubMed |
description | BACKGROUND: Woolly Hair is an uncommon congenital anomaly of the scalp hair presenting with strongly coiled hair involving a localized area of the scalp or covering the entire side and occurring in non-black people. Isolated or localized wooly hair is usually benign and is not related to other disorders and/or complications. On the contrary, the generalized type may be related to disorders and syndromes affecting heart, cutis, liver and gastrointestinal organs. Among the syndromes presenting with wooly hair, the most known are the Naxos syndrome, the Carvajal-Huerta syndrome, the wooly hair/hypotrichosis, the ectodermal dysplasia-skin fragility, the tricho-hepato-enteric syndrome. CASE PRESENTATION: To our knowledge, no cases of wooly hair syndromes has been associated to neurologic involvement. Among the clinical notes of patients admitted in the Pediatric Units of the Catania University, we have selected four individuals presenting wooly hair, who showed different clinical features and course: case 1 presenting with a localized wooly hair type; case 2, member of a family affected by WH with autosomal dominant inheritance, not associated to complications; case 3, a wooly hair patient who displayed a progressive, severe form of Rasmussen’s encephalitis with fatal evolution, and case 4, wooly hair associated to brain malformation and drug-resistant epilepsy. CONCLUSIONS: With this report, we aim to underline the wide spectrum of clinical presentation of individuals with WH and in particular we wish to give an annotation on a possible association of WH with severe neurologic disorders. |
format | Online Article Text |
id | pubmed-5667512 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-56675122017-11-08 Clinical spectrum of woolly hair: indications for cerebral involvement Pavone, Piero Falsaperla, Raffaele Barbagallo, Massimo Polizzi, Agata Praticò, Andrea D. Ruggieri, Martino Ital J Pediatr Case Report BACKGROUND: Woolly Hair is an uncommon congenital anomaly of the scalp hair presenting with strongly coiled hair involving a localized area of the scalp or covering the entire side and occurring in non-black people. Isolated or localized wooly hair is usually benign and is not related to other disorders and/or complications. On the contrary, the generalized type may be related to disorders and syndromes affecting heart, cutis, liver and gastrointestinal organs. Among the syndromes presenting with wooly hair, the most known are the Naxos syndrome, the Carvajal-Huerta syndrome, the wooly hair/hypotrichosis, the ectodermal dysplasia-skin fragility, the tricho-hepato-enteric syndrome. CASE PRESENTATION: To our knowledge, no cases of wooly hair syndromes has been associated to neurologic involvement. Among the clinical notes of patients admitted in the Pediatric Units of the Catania University, we have selected four individuals presenting wooly hair, who showed different clinical features and course: case 1 presenting with a localized wooly hair type; case 2, member of a family affected by WH with autosomal dominant inheritance, not associated to complications; case 3, a wooly hair patient who displayed a progressive, severe form of Rasmussen’s encephalitis with fatal evolution, and case 4, wooly hair associated to brain malformation and drug-resistant epilepsy. CONCLUSIONS: With this report, we aim to underline the wide spectrum of clinical presentation of individuals with WH and in particular we wish to give an annotation on a possible association of WH with severe neurologic disorders. BioMed Central 2017-11-02 /pmc/articles/PMC5667512/ /pubmed/29096685 http://dx.doi.org/10.1186/s13052-017-0417-1 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Case Report Pavone, Piero Falsaperla, Raffaele Barbagallo, Massimo Polizzi, Agata Praticò, Andrea D. Ruggieri, Martino Clinical spectrum of woolly hair: indications for cerebral involvement |
title | Clinical spectrum of woolly hair: indications for cerebral involvement |
title_full | Clinical spectrum of woolly hair: indications for cerebral involvement |
title_fullStr | Clinical spectrum of woolly hair: indications for cerebral involvement |
title_full_unstemmed | Clinical spectrum of woolly hair: indications for cerebral involvement |
title_short | Clinical spectrum of woolly hair: indications for cerebral involvement |
title_sort | clinical spectrum of woolly hair: indications for cerebral involvement |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5667512/ https://www.ncbi.nlm.nih.gov/pubmed/29096685 http://dx.doi.org/10.1186/s13052-017-0417-1 |
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