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Let Time Teach You: A Case Report of a Double Diagnosis of 17P Duplication and Ehlers-Danlos Syndrome.
Castronovo, Paola; Aleo, Sebastiano; Seresini, Agostino; Grilli, Federico; Brunati, Emilio; Marchisio, Paola; Guez, Sophie; Milani, Donatella.
Afiliação
  • Castronovo P; Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Medical Genetics Laboratory, 20122 Milan, Italy.
  • Aleo S; Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Occupational Health Unit, 20122 Milan, Italy.
  • Seresini A; Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, 20122 Milan, Italy.
  • Grilli F; Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Medical Genetics Laboratory, 20122 Milan, Italy.
  • Brunati E; Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, 20122 Milan, Italy.
  • Marchisio P; Centro di Neuroriabilitazione Pediatrica, Casa di Cura Privata del Policlinico, 20144 Milan, Italy.
  • Guez S; Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, 20122 Milan, Italy.
  • Milani D; Università degli Studi di Milano, 20122, Milan, Italy.
Genes (Basel) ; 13(12)2022 11 23.
Article em En | MEDLINE | ID: mdl-36553464
Kyphoscoliotic Ehlers-Danlos syndrome and 17p13.3 microduplication share multiple clinical features such as muscle hypotonia, cleft palate, and growth impairment. This paper describes a patient who was first diagnosed with the duplication and a decade later also with FKBP14-kEDS. The latter was initially overlooked due to the pathogenic significance attributed to the duplication and to the fact that, at the time of the first diagnosis, this specific form of kEDS had yet to be discovered. The patient's progressive kyphoscoliosis and severe joint laxity were the clinical features that prompted the patient's physiatrist to reassess the genetic work-up. This extreme latency caused inaccurate management in the patient's follow-up program, which ultimately may have resulted in preventable clinical complications. This report underlines the importance of remaining up-to-date with patient status, reviewing old cases, and relying on specialist advice to reach a correct diagnosis.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Ehlers-Danlos Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Revista: Genes (Basel) Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Itália

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Ehlers-Danlos Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Revista: Genes (Basel) Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Itália