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Dual molecular diagnoses in a neurometabolic specialty clinic.
Hannah-Shmouni, Fady; Al-Shahoumi, Rashid; Brady, Lauren I; Wu, Lily; Frei, Julia; Tarnopolsky, Mark A.
Afiliação
  • Hannah-Shmouni F; Section on Endocrinology and Genetics, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, USA.
  • Al-Shahoumi R; Department of Pediatrics, McMaster University, Hamilton, Ontario, Canada.
  • Brady LI; Department of Pediatrics, McMaster University, Hamilton, Ontario, Canada.
  • Wu L; Department of Pediatrics, McMaster University, Hamilton, Ontario, Canada.
  • Frei J; Department of Pediatrics, McMaster University, Hamilton, Ontario, Canada.
  • Tarnopolsky MA; Department of Pediatrics, McMaster University, Hamilton, Ontario, Canada.
Am J Med Genet A ; 185(3): 766-773, 2021 03.
Article em En | MEDLINE | ID: mdl-33369152
Reports of patients with concomitant diagnoses of two inherited genetic disorders, sometimes referred to as "double trouble," have appeared intermittently in the medical literature. We report eight additional cases with dual diagnoses of two genetic conditions. All cases had a phenotype atypical for their primary diagnosis, leading to the search for a second genetic diagnosis. These cases highlight the importance of the history, physical examination and continued work-up if the phenotype of the patient falls drastically outside what has been reported with their primary diagnosis. Some of the diagnoses of the patients presented here (e.g., Myotonic Dystrophy Type 1, fascioscapulohumeral muscular dystrophy) would not have been identified by genetic testing done on a next generation sequencing backbone (e.g., panel or exome sequencing). When the clinical picture is atypical or more severe than expected the possibility of a dual diagnosis (double trouble) should be considered. Identification of a second genetic condition can impact management and genetic counseling.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Marcadores Genéticos / Testes Genéticos / Distrofia Muscular Facioescapuloumeral / Mutação / Distrofia Miotônica Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male / Newborn Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Marcadores Genéticos / Testes Genéticos / Distrofia Muscular Facioescapuloumeral / Mutação / Distrofia Miotônica Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male / Newborn Idioma: En Ano de publicação: 2021 Tipo de documento: Article