An Unusual Combination of Neurological Manifestations and Sudden Vision Loss in a Child with Familial Hyperphosphatemic Tumoral Calcinosis.

Lingappa, Lokesh; Ichikawa, Shoji; Gray, Amie K; Acton, Dena; Evans, Michael J; Madarasu, Rajsekara Chakravarthi; Kekunnaya, Ramesh; Siddaiahagari, Sirisharani

Lingappa, Lokesh; Ichikawa, Shoji; Gray, Amie K; Acton, Dena; Evans, Michael J; Madarasu, Rajsekara Chakravarthi; Kekunnaya, Ramesh; Siddaiahagari, Sirisharani.

Afiliação

Lingappa L; Department of Neurology and Hemato-Oncology, Rainbow Children's Hospital and Birthright, Hyderabad, Telangana, India.
Ichikawa S; Department of Medicine, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Gray AK; Department of Medicine, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Acton D; Department of Medicine, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Evans MJ; Department of Medicine, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Madarasu RC; Department of Nephrology, Star Hospital, Hyderabad, Telangana, India.
Kekunnaya R; Jasti V Ramanamma Children's Eye Care Centre, LV Prasad Eye Institute, Hyderabad, Telangana, India.
Siddaiahagari S; Department of Neurology and Hemato-Oncology, Rainbow Children's Hospital and Birthright, Hyderabad, Telangana, India.

Ann Indian Acad Neurol ; 22(3): 327-331, 2019.

Article em En | MEDLINE | ID: mdl-31359949

Palavras-chave

Continuous ambulatory peritoneal dialysis; familial hyperphosphatemic tumor calcinosis; primary FGF23 deficiency; sevelamer; sudden vision loss

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Ann Indian Acad Neurol Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Índia

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