X-linked recessive hypoparathyroidism is a rare, congenital form of hypoparathyroidism.
| X-linked recessive hypoparathyroidism | |
|---|---|
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| X-linked recessive manner of inheritance | |
| Specialty | Endocrinology |
Signs and symptoms
editThe signs and symptoms of X-linked recessive hypoparathyroidism are characteristic of hypoparathyroidism and its consequent hypocalcemia. They include acute symptoms, like paresthesia, twitching of the hands and feet, unconsciousness, and trouble breathing; and chronic symptoms, including seizures, tiredness, irritability, cardiac insufficiency, abnormal heart rhythms, papilledema, cataracts, calcium deposits in the brain, and loss or brittleness of hair, skin, and nails.[1]
Genetics
editThis disease is named for its inheritance, which occurs in an x-linked recessive pattern.[1]
Pathophysiology
editIn this particular form of hypoparathyroidism, the parathyroid glands are underdeveloped and therefore do not produce enough parathyroid hormone. This is caused by a mutation on the x chromosome in the region of Xq26-27.[1]
Diagnosis
editHypoparathyroidism can be diagnosed using blood tests, the Chvostek sign, and the Trousseau sign. If comorbid conditions like congenital malformations, impaired growth, and intellectual disability are present, it may be a genetic form of hypoparathyroidism; the affected gene can be determined using a DNA test.[1]
Treatment
editX-linked recessive hypoparathyroidism is treated like other forms of the disease, using calcium and vitamin D supplementation. Supplementation with parathyroid hormone is another treatment option.[1]