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Tenofovir-associated Fanconi syndrome and hypophosphatemic rickets in a girl infected with HIV
(Sociedad Chilena de Pediatría, 2017)
Introduction: Tenofovir (TDF) is an inhibitor of reverse transcriptase nucleotide analogue, although it has good tolerability and high anti-retroviral activity, its effect on the kidney has been a concern. Objective: To ...
An Uncommon Cause of Hypophosphatemic Rickets
(Karger, 2016)
Dental alterations associated with X-linked hypophosphatemic rickets
(Lippincott Williams & WilkinsPhiladelphiaEUA, 2004)
Hypophosphatemic osteomalacia acquired after renal transplantation: a a cause of severe osteoporosis Osteomalacia hipofosfémica adquirida post-trasplante renal: una causa de osteoporosis grave.
(1995)
Renal osteodystrophy improves after renal transplantation but, after the procedure, other forms of bone disease emerge. We report a male patient that received a renal allograft four years before, who consulted for low back ...
Consenso de expertos colombianos sobre recomendaciones basadas en evidencia para el diagnóstico, tratamiento y seguimiento del raquitismo hipofosfatémico ligado al cromosoma X (RHLX)
(Research Square Company, 2023)
Background: X-linked hypophosphatemic rickets is a hereditary disease that generates alterations in bone
mineral homeostasis. The morbidity of the condition has been variable in previous decades and even
contradictory, ...
Síndrome de Fanconi y raquitismo hipofosfatémico asociado al uso de tenofovir en una niña infectada con VIH
(Sociedad Chilena de Pediatría, 2017)
Introducción: El tenofovir (TDF) es un inhibidor de la transcriptasa reversa análogo de nucleótidos,
aunque tiene buena tolerabilidad y alta actividad antirretroviral, su efecto sobre el riñón ha sido un
motivo de ...
Oncogenic hypophosphatemic osteomalacia associated with a nasal hemangiopericytoma
(LIPPINCOTT WILLIAMS & WILKINS, 2003)
We report a patient with a nasal hemangiopericytoma associated with an oncogenic hypophosphartemic osteomalacia (OHO). This syndrome results from tumor products that decrease renal tubular phosphate resorption, leading to ...
Clinical follow up of Chilean patients with tyrosinemia type 1 treated with 2-(2-nitro-4-trifl uoromethylbenzoyl)- 1,3-ciclohexanedione (NTBC) Evolución clínica de pacientes chilenos con tirosinemia tipo I tratados con 2-(2-nitro-4-trifluorometilbenzoil)-
(2012)
Background: Tyrosinemia type I is an inborn error of metabolism due to defi ciency of fumarilacetoacetase. Acute presentation is with liver failure, hypophosphatemic rickets and peripheral neuropathy. Chronic presentation ...
Osteomalacia Tumoral
(Asociación Argentina de Osteología y Metabolismo Mineral, 2008-12)
La osteomalacia tumoral (OT) es un síndrome paraneoplásico en el cual el paciente presenta dolor óseo, fracturas y debilidad muscular. Es producido principalmente por una elevación de los niveles en sangre del factor de ...
Osteomalacia oncogénica: presentación de dos casosOncogenic osteomalacia: report of two cases
(Medicina (Buenos Aires), 2015-02)
La osteomalacia oncogénica es una enfermedad rara. Existen descriptos alrededor de 337 casos. Es ocasionada por un tumor productor del factor de crecimiento fibroblástico 23 (FGF-23), hormona que disminuye la reabsorción ...