Familial isolated hypoparathyroidism (Q56223): Difference between revisions
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Hipoparatireoidismo familiar isolado é um grupo heterogêneo e raro de transtornos metabólicos caracterizado por metabolismo anormal do cálcio devido secreção deficiente de paratormônio (PTH), com outros transtornos endócrinos ou defeitos do desenvolvimento, de herança autossômica dominante ou recessiva. | |||
| description / en | description / en | ||
Familial isolated hypoparathyroidism is a rare heterogeneous group of metabolic disorders characterised by abnormal calcium metabolism due to deficient secretion of parathormone (PTH), without other endocrine disorders or developmental defects, with autosomal dominant or recessive inheritance. | |||
Revision as of 03:54, 14 August 2026
Familial isolated hypoparathyroidism is a rare heterogeneous group of metabolic disorders characterised by abnormal calcium metabolism due to deficient secretion of parathormone (PTH), without other endocrine disorders or developmental defects, with autosomal dominant or recessive inheritance.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1079633828 |
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| English | Familial isolated hypoparathyroidism |
Familial isolated hypoparathyroidism is a rare heterogeneous group of metabolic disorders characterised by abnormal calcium metabolism due to deficient secretion of parathormone (PTH), without other endocrine disorders or developmental defects, with autosomal dominant or recessive inheritance. |
