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A new case of Turnpenny-Fry syndrome.
Ercoskun, Pelin; Yuce Kahraman, Cigdem; Adanur Saglam, Kübra; Kanjee, Momen; Tatar, Abdulgani.
Afiliación
  • Ercoskun P; Department of Medical Genetics, Faculty of Medicine, Ataturk University, Erzurum, Turkey.
  • Yuce Kahraman C; Department of Medical Genetics, Faculty of Medicine, Ataturk University, Erzurum, Turkey.
  • Adanur Saglam K; Department of Medical Genetics, Faculty of Medicine, Ataturk University, Erzurum, Turkey.
  • Kanjee M; Department of Medical Genetics, Faculty of Medicine, Ataturk University, Erzurum, Turkey.
  • Tatar A; Department of Medical Genetics, Faculty of Medicine, Ataturk University, Erzurum, Turkey.
Am J Med Genet A ; 188(2): 688-691, 2022 02.
Article en En | MEDLINE | ID: mdl-34750959
Turnpenny-Fry syndrome is a very rare genetic disorder characterized by intellectual disability, developmental delay, facial dysmorphism, and skeletal abnormalities. Mutations of the PCGF2 gene are responsible for Turnpenny-Fry syndrome. This gene encodes the polycomb group ring finger 2 protein that is broadly expressed in various human tissues. To date, only 13 patients with Turnpenny-Fry syndrome have been reported. Our patient was referred to our clinic for neuromotor retardation and dysmorphic features. Whole exome sequencing (WES) was performed from the peripheral blood sample of the patient. WES revealed a heterozygous mutation in the PCGF2 gene. To the best of our knowledge, we reported the 14th patient with Turnpenny-Fry syndrome and the first from Turkey, who had new findings.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Discapacidad Intelectual / Anomalías Musculoesqueléticas Tipo de estudio: Diagnostic_studies Límite: Humans País/Región como asunto: Asia Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2022 Tipo del documento: Article País de afiliación: Turquía Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Discapacidad Intelectual / Anomalías Musculoesqueléticas Tipo de estudio: Diagnostic_studies Límite: Humans País/Región como asunto: Asia Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2022 Tipo del documento: Article País de afiliación: Turquía Pais de publicación: Estados Unidos