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Familial factors affect hair loss types in Koreans, with M type in men, L type in women, and paternal factors influencing male hair loss more.

Treatment with dutasteride, minoxidil, and artificial hair transplantation improved appearance but caused folliculitis.

The conclusion is that hair loss from CCCA may be genetic and not solely caused by hair grooming practices.

Frontal fibrosing alopecia in families shows similar signs to individual cases and may have a genetic link.

A boy with a rare form of early puberty caused by a new gene mutation responded well to treatment aimed at reducing testosterone and preserving adult height.

Frontal fibrosing alopecia has occurred in two related male families.

A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

HIV-positive pregnant women are more likely to experience severe bleeding, and a pregnant woman with familial hypertriglyceridemia had a successful early delivery with special care.

Two young siblings experienced hair loss without hormone issues or other skin problems.

Familial frontal fibrosing alopecia is rare, mostly affects women, and often occurs between sisters or mother-daughter pairs.

A girl inherited excessive body hair from her mother and grandmother.

The document concludes that the girl's hairlessness is likely inherited from her parents.

Premature hair graying in the face may be influenced by genetics and environment.

Two siblings were the first reported cases of inheriting both eye coloboma and loose anagen syndrome together.

A new genetic mutation in the TRPV3 gene causes Olmsted-like syndrome in a Mongolian family.

Coats' Plus is a genetic disorder with eye abnormalities, brain calcification, poor growth, bone and skin issues, and movement disorders.

Newborn acne may be linked to family history of high male hormone levels.

Cantú syndrome may be linked to pituitary adenomas.

A 17-year-old girl and her brothers have a rare hair condition with long eyelashes, thick eyebrows, and easily pluckable hair.

A mother and her two daughters got a skin infection from their cat.

The document concludes that managing Dunnigan-Type Familial Partial Lipodystrophy involves treating associated health issues and using medications like metformin and leptin replacement.

Women with PCOS often have hirsutism and skin changes, which indicate a need for metabolic health checks.

The document describes a woman with familial Parkinson's disease due to a genetic mutation, showing severe symptoms and poor response to treatment, and suggests finasteride may help reduce symptoms in Tourette syndrome.

The document concludes that detailed clinical descriptions of seven family cases help understand dominant dystrophic epidermolysis bullosa's symptoms and inheritance.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

Monilethrix causes brittle hair and hair loss, and it runs in families.

A subtle androgen receptor abnormality can allow normal male development and sometimes fertility despite partial androgen resistance.

Certain genetic markers, especially the MICA gene, are linked to alopecia areata.

RET mutation is important in familial medullary thyroid carcinoma, and BRAF mutation in papillary thyroid carcinoma is linked to more aggressive cancer and higher death rates.