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Consanguineous couple with SDHD gene mutations: Diagnosis, treatment, and implications of family genetic testing.
Braegelmann, Johanna; Mathew, Annie; Führer-Sakel, Dagmar; Lahner, Harald.
Afiliación
  • Braegelmann J; Department of Endocrinology, Diabetes and Metabolism and Division of Laboratory Research, Endocrine Tumor Center at WTZ and Member of EURACAN, ENETS Center of Excellence University Hospital Essen Essen Germany.
  • Mathew A; Department of Endocrinology, Diabetes and Metabolism and Division of Laboratory Research, Endocrine Tumor Center at WTZ and Member of EURACAN, ENETS Center of Excellence University Hospital Essen Essen Germany.
  • Führer-Sakel D; Department of Endocrinology, Diabetes and Metabolism and Division of Laboratory Research, Endocrine Tumor Center at WTZ and Member of EURACAN, ENETS Center of Excellence University Hospital Essen Essen Germany.
  • Lahner H; Department of Endocrinology, Diabetes and Metabolism and Division of Laboratory Research, Endocrine Tumor Center at WTZ and Member of EURACAN, ENETS Center of Excellence University Hospital Essen Essen Germany.
Clin Case Rep ; 12(4): e8572, 2024 Apr.
Article en En | MEDLINE | ID: mdl-38585582
ABSTRACT
The newly published clinical consensus guideline on the management of PGL/PCC is helpful for decision-making for diagnostics and treatment. Still, the treatment of patients with SDHD gene mutations requires an individual approach and those patients belong to multiprofessional teams. It is often assumed that spouses are genetically unrelated. However, the genetic relationships between spouses should always be examined empathetically and impartially.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Clin Case Rep Año: 2024 Tipo del documento: Article Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Clin Case Rep Año: 2024 Tipo del documento: Article Pais de publicación: Reino Unido