Visão selecionada em Inglês
Descritor em português: | Síndrome de Sotos | ||||
Descritor em inglês: | Sotos Syndrome | ||||
Descritor em espanhol: |
Síndrome de Sotos
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Descritor em francês: | Syndrome de Sotos | ||||
Termo(s) alternativo(s): |
Cerebral Gigantism Cerebral Gigantisms Gigantism, Cerebral Gigantisms, Cerebral Sequence, Sotos Soto Syndrome Soto's Syndrome Sotos Sequence Sotos' Syndrome Syndrome, Sotos Syndrome, Sotos' |
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Código(s) hierárquico(s): |
C16.131.077.889 C16.131.260.905 C16.320.180.905 |
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Identificador Único RDF: | https://id.nlm.nih.gov/mesh/D058495 | ||||
Nota de escopo: | Congenital or postnatal overgrowth syndrome most often in height and occipitofrontal circumference with variable delayed motor and cognitive development. Other associated features include advanced bone age, seizures, NEONATAL JAUNDICE; HYPOTONIA; and SCOLIOSIS. It is also associated with increased risk of developing neoplasms in adulthood. Mutations in the NSD1 protein and its HAPLOINSUFFICIENCY are associated with the syndrome. |
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Qualificadores permitidos: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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Indexação Anterior: |
Acromegaly (1977-2010) Gigantism (1977-2010) |
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Nota MeSH pública: | 2011 |
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Nota histórica: | 2011 |
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Veja também os descritores: |
Fetal Macrosomia
MeSH Gigantism MeSH | ||||
Identificador DeCS: | 53997 | ||||
ID do descritor: | D058495 | ||||
Documentos indexados na Biblioteca Virtual em Saúde (BVS): | Clique aqui para acessar os documentos da BVS | ||||
Data de estabelecimento: | 01/01/2011 | ||||
Data de entrada: | 25/06/2010 | ||||
Data de revisão: | 08/07/2013 |
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Sotos Syndrome
- Conceito preferido
Identificador do conceito |
M0542875 |
Nota de escopo | Congenital or postnatal overgrowth syndrome most often in height and occipitofrontal circumference with variable delayed motor and cognitive development. Other associated features include advanced bone age, seizures, NEONATAL JAUNDICE; HYPOTONIA; and SCOLIOSIS. It is also associated with increased risk of developing neoplasms in adulthood. Mutations in the NSD1 protein and its HAPLOINSUFFICIENCY are associated with the syndrome. |
Termo preferido | Sotos Syndrome |
Termo(s) alternativo(s) |
Cerebral Gigantism Cerebral Gigantisms Gigantism, Cerebral Gigantisms, Cerebral Sequence, Sotos Soto Syndrome Soto's Syndrome Sotos Sequence Sotos' Syndrome Syndrome, Sotos Syndrome, Sotos' |
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