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A de novo TBX3 mutation presenting as dorsalization of the little fingers: A forme fruste phenotype of ulnar-mammary syndrome.
Al-Qattan, Mohammad M; Maddirevula, Sateesh; Alkuraya, Fowzan S.
Afiliação
  • Al-Qattan MM; Division of Plastic Surgery at King Saud University, Riyadh, Saudi Arabia; Division of Plastic Surgery at King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Maddirevula S; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Alkuraya FS; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia; Department of Anatomy and Cell Biology, College of Medicine, Alfaisal University, Riyadh, Saudi Arabia. Electronic address: falkuraya@kfshrc.edu.sa.
Eur J Med Genet ; 63(1): 103615, 2020 Jan.
Article em En | MEDLINE | ID: mdl-30654152
Ulnar-mammary syndrome (UMS) is a rare syndromic limb malformation caused by heterozygous mutations in TBX3. The name highlights the two commonly involved body parts i.e. mammary gland and ulnar ray of the upper limbs, although a more extensive systemic involvement is also known to occur. Here, we report the surprising finding of a patient with a de novo mutation in TBX3 whose clinical presentation is limited to dorsalization of both little fingers and slightly deep 4th web spaces. We review the literature to confirm that this should be considered as a forme fruste phenotype of UMS.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ulna / Anormalidades Múltiplas / Doenças Mamárias / Deformidades Congênitas dos Membros / Proteínas com Domínio T Limite: Child / Female / Humans Idioma: En Revista: Eur J Med Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Arábia Saudita

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ulna / Anormalidades Múltiplas / Doenças Mamárias / Deformidades Congênitas dos Membros / Proteínas com Domínio T Limite: Child / Female / Humans Idioma: En Revista: Eur J Med Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Arábia Saudita