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Familial campomelic dysplasia due to maternal germinal mosaicism.
Higeta, Daisuke; Yamaguchi, Rie; Takagi, Takeshi; Nishimura, Gen; Sameshima, Kiyoko; Saito, Kayoko; Minegishi, Takashi.
Afiliação
  • Higeta D; Department of Obstetrics and Gynecology, Gunma University, Graduate School of Medicine, Gunma, Japan.
  • Yamaguchi R; Department of Obstetrics and Gynecology, Japan Community Health Care Organization, Gunma Chuo Hospital, Gunma, Japan.
  • Takagi T; Department of Pediatrics, Hamamatsu University School of Medicine, Hamamatsu, Japan.
  • Nishimura G; Department of Obstetrics, Gunma Children's Medical Center, Gunma, Japan.
  • Sameshima K; Intractable Disease Center, Saitama Medical University Hospital, Saitama, Japan.
  • Saito K; Department of Pediatrics, Minamikyusyu National Hospital, Kagoshima, Japan.
  • Minegishi T; Institute of Medical Genetics, Tokyo Women's Medical University, Tokyo, Japan.
Congenit Anom (Kyoto) ; 58(6): 194-197, 2018 Nov.
Article em En | MEDLINE | ID: mdl-29542186
Campomelic dysplasia is an autosomal dominant skeletal dysplasia caused by heterozygous SOX9 mutations. Most patients are sporadic due to a de novo mutation. Familial campomelic dysplasia is very rare. We report on a familial campomelic dysplasia caused by maternal germinal mosaicism. Two siblings showed the classic campomelic dysplasia phenotype with a novel SOX9 mutation (NM_000346.3: c.441delC, p.(Asn147Lysfs*36)). Radiological examination of the mother showed mild skeletal changes. Then, her somatic mosaicism of the mutation was ascertained. This is the first report of molecularly confirmed maternal germinal mosaicism for a SOX9 mutation. We suggest that a meticulous clinical examination of the parents, even if they are superficially healthy, is needed to avoid overlooking germinal mosaicism of SOX9 mutations.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Mutação em Linhagem Germinativa / Displasia Campomélica / Herança Materna / Mosaicismo Tipo de estudo: Diagnostic_studies Limite: Female / Humans / Male Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Mutação em Linhagem Germinativa / Displasia Campomélica / Herança Materna / Mosaicismo Tipo de estudo: Diagnostic_studies Limite: Female / Humans / Male Idioma: En Ano de publicação: 2018 Tipo de documento: Article