Xeroderma Pigmentosum with Severe Neurological Manifestations/De Sanctis–Cacchione Syndrome and a Novel XPC Mutation

ABSTRACT: Several genetic disorders caused by defective nucleotide excision repair that affect the skin and the nervous system have been described, including Xeroderma Pigmentosum (XP), De Sanctis–Cacchione syndrome (DSC), Cockayne syndrome, and Trichothiodystrophy. Cutaneous photosensitivity with a...

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Autores:
Uribe Bojanini, Esteban
Hernández Quiceno, Sara
Cock Rada, Alicia María
Tipo de recurso:
Article of journal
Fecha de publicación:
2017
Institución:
Universidad de Antioquia
Repositorio:
Repositorio UdeA
Idioma:
eng
OAI Identifier:
oai:bibliotecadigital.udea.edu.co:10495/23344
Acceso en línea:
http://hdl.handle.net/10495/23344
Palabra clave:
Ictiosis
Ichthyosis
Síndrome de Cockayne
Cockayne Syndrome
Síndromes de Tricotiodistrofia
Trichothiodystrophy Syndromes
Rights
openAccess
License
http://creativecommons.org/licenses/by/2.5/co/
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network_acronym_str UDEA2
network_name_str Repositorio UdeA
repository_id_str
dc.title.spa.fl_str_mv Xeroderma Pigmentosum with Severe Neurological Manifestations/De Sanctis–Cacchione Syndrome and a Novel XPC Mutation
title Xeroderma Pigmentosum with Severe Neurological Manifestations/De Sanctis–Cacchione Syndrome and a Novel XPC Mutation
spellingShingle Xeroderma Pigmentosum with Severe Neurological Manifestations/De Sanctis–Cacchione Syndrome and a Novel XPC Mutation
Ictiosis
Ichthyosis
Síndrome de Cockayne
Cockayne Syndrome
Síndromes de Tricotiodistrofia
Trichothiodystrophy Syndromes
title_short Xeroderma Pigmentosum with Severe Neurological Manifestations/De Sanctis–Cacchione Syndrome and a Novel XPC Mutation
title_full Xeroderma Pigmentosum with Severe Neurological Manifestations/De Sanctis–Cacchione Syndrome and a Novel XPC Mutation
title_fullStr Xeroderma Pigmentosum with Severe Neurological Manifestations/De Sanctis–Cacchione Syndrome and a Novel XPC Mutation
title_full_unstemmed Xeroderma Pigmentosum with Severe Neurological Manifestations/De Sanctis–Cacchione Syndrome and a Novel XPC Mutation
title_sort Xeroderma Pigmentosum with Severe Neurological Manifestations/De Sanctis–Cacchione Syndrome and a Novel XPC Mutation
dc.creator.fl_str_mv Uribe Bojanini, Esteban
Hernández Quiceno, Sara
Cock Rada, Alicia María
dc.contributor.author.none.fl_str_mv Uribe Bojanini, Esteban
Hernández Quiceno, Sara
Cock Rada, Alicia María
dc.contributor.researchgroup.spa.fl_str_mv Genética Médica
dc.subject.decs.none.fl_str_mv Ictiosis
Ichthyosis
Síndrome de Cockayne
Cockayne Syndrome
Síndromes de Tricotiodistrofia
Trichothiodystrophy Syndromes
topic Ictiosis
Ichthyosis
Síndrome de Cockayne
Cockayne Syndrome
Síndromes de Tricotiodistrofia
Trichothiodystrophy Syndromes
description ABSTRACT: Several genetic disorders caused by defective nucleotide excision repair that affect the skin and the nervous system have been described, including Xeroderma Pigmentosum (XP), De Sanctis–Cacchione syndrome (DSC), Cockayne syndrome, and Trichothiodystrophy. Cutaneous photosensitivity with an increased risk of skin malignancy is a common feature of these disorders, but clinical manifestations commonly overlap these syndromes. Several genes have been found to be altered in these pathologies, but we lack more genotype-phenotype correlations in order to make an accurate diagnosis. Very few cases of DSC syndrome have been reported in the literature. We present a case of a 12-year-old Colombian male, with multiple skin lesions in sun-exposed areas from the age of 3 months and a history of 15 skin cancers. He also displayed severe neurologic abnormalities (intellectual disability, ataxia, altered speech, and hyperreflexia), short stature, and microcephaly, which are features associated with DSC. Genetic testing revealed a novel germline mutation in the XP-C gene (c.547A>T). This is the first case of an XP-C mutation causing De Sanctis–Cacchione syndrome. Multigene panel testing is becoming more widely available and accessible in the clinical setting and will help rapidly unveil the molecular etiology of these rare genetic disorders.
publishDate 2017
dc.date.issued.none.fl_str_mv 2017
dc.date.accessioned.none.fl_str_mv 2021-10-21T14:22:46Z
dc.date.available.none.fl_str_mv 2021-10-21T14:22:46Z
dc.type.spa.fl_str_mv Reporte de caso
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dc.identifier.issn.none.fl_str_mv 1687-9627
dc.identifier.uri.none.fl_str_mv http://hdl.handle.net/10495/23344
dc.identifier.doi.none.fl_str_mv 10.1155/2017/7162737
dc.identifier.eissn.none.fl_str_mv 1687-9635
identifier_str_mv 1687-9627
10.1155/2017/7162737
1687-9635
url http://hdl.handle.net/10495/23344
dc.language.iso.spa.fl_str_mv eng
language eng
dc.relation.ispartofjournalabbrev.spa.fl_str_mv Case. Rep. Med.
dc.relation.citationendpage.spa.fl_str_mv 8
dc.relation.citationstartpage.spa.fl_str_mv 1
dc.relation.citationvolume.spa.fl_str_mv 2017
dc.relation.ispartofjournal.spa.fl_str_mv Case Reports in Medicine
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dc.publisher.spa.fl_str_mv Hindawi
dc.publisher.place.spa.fl_str_mv Nueva York, Estados Unidos
institution Universidad de Antioquia
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spelling Uribe Bojanini, EstebanHernández Quiceno, SaraCock Rada, Alicia MaríaGenética Médica2021-10-21T14:22:46Z2021-10-21T14:22:46Z20171687-9627http://hdl.handle.net/10495/2334410.1155/2017/71627371687-9635ABSTRACT: Several genetic disorders caused by defective nucleotide excision repair that affect the skin and the nervous system have been described, including Xeroderma Pigmentosum (XP), De Sanctis–Cacchione syndrome (DSC), Cockayne syndrome, and Trichothiodystrophy. Cutaneous photosensitivity with an increased risk of skin malignancy is a common feature of these disorders, but clinical manifestations commonly overlap these syndromes. Several genes have been found to be altered in these pathologies, but we lack more genotype-phenotype correlations in order to make an accurate diagnosis. Very few cases of DSC syndrome have been reported in the literature. We present a case of a 12-year-old Colombian male, with multiple skin lesions in sun-exposed areas from the age of 3 months and a history of 15 skin cancers. He also displayed severe neurologic abnormalities (intellectual disability, ataxia, altered speech, and hyperreflexia), short stature, and microcephaly, which are features associated with DSC. Genetic testing revealed a novel germline mutation in the XP-C gene (c.547A>T). This is the first case of an XP-C mutation causing De Sanctis–Cacchione syndrome. Multigene panel testing is becoming more widely available and accessible in the clinical setting and will help rapidly unveil the molecular etiology of these rare genetic disorders.COL00067328application/pdfengHindawiNueva York, Estados Unidoshttp://creativecommons.org/licenses/by/2.5/co/https://creativecommons.org/licenses/by/4.0/info:eu-repo/semantics/openAccesshttp://purl.org/coar/access_right/c_abf2Xeroderma Pigmentosum with Severe Neurological Manifestations/De Sanctis–Cacchione Syndrome and a Novel XPC MutationReporte de casohttp://purl.org/coar/resource_type/c_6501http://purl.org/coar/resource_type/c_2df8fbb1https://purl.org/redcol/resource_type/ARTCASOhttp://purl.org/coar/version/c_970fb48d4fbd8a85info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionIctiosisIchthyosisSíndrome de CockayneCockayne SyndromeSíndromes de TricotiodistrofiaTrichothiodystrophy SyndromesCase. Rep. 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