Familial hypomagnesaemia - hypercalciuria - nephrocalcinosis (Q99740): Difference between revisions

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A hipomagnesemia familiar com hipercalciúria e nefrocalcinose é uma doença renal progressiva, caracterizada por hipomagnesemia, hipercalciúria e nefrocalcinose. Infecções recorrentes do trato urinário e cálculos renais são freqüentemente observados e, em um terço a metade dos pacientes, anormalidades oculares como nistagmo horizontal, miopia, calcificações corneanas e coriorretinite são observadas.
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Familial hypomagnesemia with hypercalciuria and nephrocalcinosis is a progressive renal disease, characterised by hypomagnesemia, hypercalciuria and nephrocalcinosis. Recurrent urinary tract infections and kidney stones are often observed, and in one third to half of the patients, ocular abnormalities such as horizontal nystagmus, myopia, corneal calcifications and chorioretinitis are observed.

Revision as of 16:24, 16 August 2026

Familial hypomagnesemia with hypercalciuria and nephrocalcinosis is a progressive renal disease, characterised by hypomagnesemia, hypercalciuria and nephrocalcinosis. Recurrent urinary tract infections and kidney stones are often observed, and in one third to half of the patients, ocular abnormalities such as horizontal nystagmus, myopia, corneal calcifications and chorioretinitis are observed.
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    Familial hypomagnesaemia - hypercalciuria - nephrocalcinosis
    Familial hypomagnesemia with hypercalciuria and nephrocalcinosis is a progressive renal disease, characterised by hypomagnesemia, hypercalciuria and nephrocalcinosis. Recurrent urinary tract infections and kidney stones are often observed, and in one third to half of the patients, ocular abnormalities such as horizontal nystagmus, myopia, corneal calcifications and chorioretinitis are observed.

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