Familial multiple lipomatosis is a rare, benign genetic condition that primarily affects the skin and subcutaneous tissues. It is characterized by the...

Familial multiple nevi flammei is a congenital vascular malformation of the skin that is evident as flat, reddish-purplish birthmarks caused by dilate...

Familial nonmedullary thyroid carcinoma is a rare form of thyroid cancer that occurs in families without being part of a broader syndrome. It primaril...

Familial or sporadic hemiplegic migraine is a rare type of migraine distinguished by the presence of temporary motor weakness during the aura phase. T...

Familial ovarian cancer is a form of ovarian cancer that happens because of an inherited change in the genome. This means that the alteration in the g...

Familial ovarian carcinoma refers to ovarian cancer that appears in relatives of individuals with a history of the disease. This condition affects the...

Familial pancreatic carcinoma is a form of pancreatic cancer that occurs in families with two or more first‐degree relatives affected by the disease....

Familial papillary or follicular thyroid carcinoma is a form of thyroid cancer that occurs within families and is distinguished by tumors that are oft...

Familial papillary thyroid carcinoma with renal papillary neoplasia is an extremely rare inherited tumor syndrome that falls within the familial nonme...

Familial partial epilepsy is an inherited form of epilepsy that primarily affects the electrical activity in specific regions of the brain. This condi...

Familial partial lipodystrophy is a group of rare genetic syndromes characterized by an abnormal loss of fat from the limbs and buttocks, often presen...