A rare intrauterine onset growth retardation syndrome caused by mosaic 19p13.3 microduplication: evaluation of GH/IGF- 1 axis and GH therapy response.

Özer, Emre; Karaman, Birsen; Günes, Nilay; Evliyaoglu, Olcay; Tüysüz, Beyhan

Özer, Emre; Karaman, Birsen; Günes, Nilay; Evliyaoglu, Olcay; Tüysüz, Beyhan.

Afiliación

Özer E; Divisions of Pediatric Genetics, Istanbul University Cerrahpasa Faculty of Medicine, Istanbul, Turkey.
Karaman B; Division of Medical Genetics, Istanbul University Faculty of Medicine, Istanbul, Turkey.
Günes N; Divisions of Pediatric Genetics, Istanbul University Cerrahpasa Faculty of Medicine, Istanbul, Turkey.
Evliyaoglu O; Divisions of Pediatric Endocrinology, Department of Pediatrics, Istanbul University Cerrahpasa Faculty of Medicine, Istanbul, Turkey.
Tüysüz B; Divisions of Pediatric Genetics, Istanbul University Cerrahpasa Faculty of Medicine, Istanbul, Turkey.

Turk J Pediatr ; 63(1): 174-180, 2021.

Article en En | MEDLINE | ID: mdl-33686842

Asunto(s)

Discapacidad Intelectual; Microcefalia; Niño; Femenino; Retardo del Crecimiento Fetal; Hormona del Crecimiento/uso terapéutico; Humanos; Discapacidad Intelectual/genética; Síndrome

Palabras clave

19p13.3 microduplication; PIAS4; growth hormone; intrauterine growth retardation; microcephaly

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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Discapacidad Intelectual / Microcefalia Límite: Child / Female / Humans Idioma: En Revista: Turk J Pediatr Año: 2021 Tipo del documento: Article País de afiliación: Turquía

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