Glaudemans type isolated autosomal dominant hypomagnesaemia (Q99739): Difference between revisions
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Hipomagnesemia autossômica dominante isolada, do tipo Glaudemans, é uma forma de hipomagnesemia primária familiar, caracterizada por baixos valores de magnésio sérico, mas valores normais de magnésio urinário. As características clínicas típicas são câimbras musculares recorrentes, episódios de tetania, tremor e fraqueza muscular, especialmente nos membros distais. A doença é potencialmente fatal. | |||||||||||||||
| description / en | description / en | ||||||||||||||
Isolated autosomal dominant hypomagnesemia, Glaudemans type is a form of familial primary hypomagnesemia, characterised by low serum magnesium values but normal urinary magnesium values. The typical clinical features are recurrent muscle cramps, tetanic episodes, tremor, and muscle weakness, especially in distal limbs. The disease is potentially fatal. | |||||||||||||||
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| Property / Canonical URI: https://id.who.int/icd/entity/1038958214 / rank | |||||||||||||||
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CID11:ID_1038958214 | |||||||||||||||
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dki-india-ID_1038958214 | |||||||||||||||
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| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
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15 August 2026
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Latest revision as of 16:24, 16 August 2026
Isolated autosomal dominant hypomagnesemia, Glaudemans type is a form of familial primary hypomagnesemia, characterised by low serum magnesium values but normal urinary magnesium values. The typical clinical features are recurrent muscle cramps, tetanic episodes, tremor, and muscle weakness, especially in distal limbs. The disease is potentially fatal.
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| default for all languages | ID_1038958214 |
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| English | Glaudemans type isolated autosomal dominant hypomagnesaemia |
Isolated autosomal dominant hypomagnesemia, Glaudemans type is a form of familial primary hypomagnesemia, characterised by low serum magnesium values but normal urinary magnesium values. The typical clinical features are recurrent muscle cramps, tetanic episodes, tremor, and muscle weakness, especially in distal limbs. The disease is potentially fatal. |
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CID11:ID_1038958214
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dki-india-ID_1038958214
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Concluído
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15 August 2026
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