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Uncombable hair syndrome causes frizzy hair and can affect the nervous system, eyes, and ears, often co-occurring with other hair, skin, nail, and teeth conditions, and is linked to three specific gene mutations.

A new mutation in the HR gene causes hair loss in a specific family.

PCOS is a condition causing irregular periods, excess male hormones, and infertility, often managed by targeting insulin resistance and specific symptoms.

TRPV3 could be a target for treating pain, skin disorders, and hair problems, but more research is needed to create effective drugs.

Fibroblast growth factor receptor signaling controls cell development and repair, and its malfunction can cause disorders and cancer, but it also offers potential for targeted therapies.

The protein FLCN is involved in cellular cleanup and is regulated by ULK1.

A TP63 gene mutation causes significant hair loss and mild skin, nail, and tooth abnormalities.

A 2-year-old boy had no hair and unusual organ placement, and it's unclear if it's genetic or coincidental.

A person was born with both a rare hairless condition and a type of birthmark, which is an uncommon combination.

The woman has a rare skin condition called follicular Dowling-Degos disease, which has limited treatment options.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

A baby had a rare case of widespread milia, which was treated and is being monitored.

A 5-year-old girl has sparse, dry, and brittle hair but is otherwise healthy.

Progeroid mouse models show signs of early aging similar to humans, helping us understand aging better.

A 4-year-old girl was diagnosed with erythrokeratodermia variabilis after other treatments failed.

Low levels of vitamin B12 and ferritin are linked to early hair graying.

AGA, a common hair loss, is caused by genetics, hormones, age, and environmental factors.

About 30% of women feel they lose too much hair, often starting before age 40, and most can't find a reason for it.

Nilotinib can cause generalized keratosis pilaris.

A woman with dermatomyositis showed rare skin symptoms, was treated successfully, and her case suggests checking for cancer in similar patients.

A woman with a rare type of dermatomyositis improved with low-dose prednisone and methotrexate.

Mutation in hairless gene may increase hair loss risk.

Mutation in hairless gene may increase hair loss risk.

Acne is linked to inflammation and insulin resistance, and is associated with various syndromes that require different treatments.

New treatments for skin conditions related to the sebaceous gland are being developed based on current research.

Men with early hair loss may have a higher risk of enlarged prostate and possibly prostate cancer due to shared hormonal factors.

DAVID syndrome is a condition with immune system and hormone deficiencies, needing early diagnosis to avoid serious complications.

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

Lifestyle changes are the main treatment for PCOS, which is a complex condition requiring early management to reduce its health impacts.

The document concludes that while white skin, nail, and mucosa diseases increase skin cancer risk, they are generally harmless, especially compared to darker pigmentation conditions.