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...
- 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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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. |
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2017 |
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2017 |
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2021-10-21T14:22:46Z |
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2021-10-21T14:22:46Z |
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1687-9627 |
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http://hdl.handle.net/10495/23344 |
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10.1155/2017/7162737 |
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1687-9635 |
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http://hdl.handle.net/10495/23344 |
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eng |
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eng |
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Case. Rep. Med. |
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2017 |
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Case Reports in Medicine |
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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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