An uncommon cause of hypophosphatemic rickets: Questions.

Koyun, Mustafa; Ertosun, Mustafa Gökhan; Aksoy, Gülsah Kaya; Çomak, Elif; Akman, Sema

Koyun, Mustafa; Ertosun, Mustafa Gökhan; Aksoy, Gülsah Kaya; Çomak, Elif; Akman, Sema.

Afiliación

Koyun M; Faculty of Medicine, Department of Pediatrics, Division of Pediatric Nephrology, Akdeniz University, Antalya, 07070, Turkey. mkoyun@akdeniz.edu.tr.
Ertosun MG; Faculty of Medicine, Department of Medical Genetics, Akdeniz University, Antalya, Turkey.
Aksoy GK; Faculty of Medicine, Department of Pediatrics, Division of Pediatric Nephrology, Akdeniz University, Antalya, 07070, Turkey.
Çomak E; Faculty of Medicine, Department of Pediatrics, Division of Pediatric Nephrology, Akdeniz University, Antalya, 07070, Turkey.
Akman S; Faculty of Medicine, Department of Pediatrics, Division of Pediatric Nephrology, Akdeniz University, Antalya, 07070, Turkey.

Pediatr Nephrol ; 38(8): 2611-2612, 2023 08.

Article en En | MEDLINE | ID: mdl-36995463

Asunto(s)

Raquitismo Hipofosfatémico Familiar; Raquitismo Hipofosfatémico; Raquitismo; Humanos; Raquitismo Hipofosfatémico Familiar/complicaciones; Raquitismo Hipofosfatémico Familiar/diagnóstico; Raquitismo Hipofosfatémico Familiar/genética; Raquitismo Hipofosfatémico/complicaciones; Raquitismo Hipofosfatémico/diagnóstico; Raquitismo/complicaciones; Raquitismo/diagnóstico

Palabras clave

Hypophosphatemic rickets; Proximal tubular dysfunction; Renal Fanconi syndrome

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Raquitismo / Raquitismo Hipofosfatémico Familiar / Raquitismo Hipofosfatémico Tipo de estudio: Diagnostic_studies Límite: Humans Idioma: En Revista: Pediatr Nephrol Asunto de la revista: NEFROLOGIA / PEDIATRIA Año: 2023 Tipo del documento: Article País de afiliación: Turquía Pais de publicación: Alemania

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