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Men might have a version of the female disease, polycystic ovarian syndrome, shown by changes in hormone levels and early baldness, but more research is needed to fully understand it.

Folliculin deficiency causes problems with cell division and positioning due to disrupted RhoA signaling and interaction with p0071.

Certain gene variations are found in people with polycystic ovary syndrome.

Frontal Fibrosing Alopecia may be linked to autoimmune diseases like Sjögren's syndrome.

Rothmund-Thomson syndrome type 2 can cause chronic, poorly healing wounds.

PAS III can cause multiple autoimmune diseases with noticeable skin issues.

Giant axonal neuropathy changes the structure of keratin in human hair.

There is no standard treatment for the rare Cronkhite–Canada syndrome, which can be fatal and lead to cancer.

SV40 T antigen in hair follicles causes abnormal hair and health issues in mice.

A boy's hair that was frizzy and hard to comb returned to normal after 9 months, possibly due to genetic factors.

The hair coat disorder in Schipperkes is similar to Alopecia X and involves increased androstenedione levels and hair cycle arrest.

Doctors should consider Netherton syndrome in patients with chronic skin and hair issues to avoid misdiagnosis.

EGFR and mTOR inhibitors may help manage Olmsted syndrome symptoms.

Skin lesions in Carney complex are likely caused by a specific group of skin cells that promote pigment production due to a genetic mutation.

A family showed a new condition with inherited hair loss and skin changes, possibly due to one genetic disorder.

People obsessed with looking young may need therapy to address deeper issues.

New genetic mutations causing hair loss were found in a Chinese family.

Birt–Hogg–Dubé syndrome is a rare genetic condition causing skin lesions, lung cysts, and a higher chance of kidney cancer.

Parental support and gender-affirming care are crucial for the mental health of transgender adolescents.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

IVIG therapy significantly improved symptoms in a patient with APS-2 and SPS.

WNT10A mutations cause varied symptoms in patients with odonto-onycho-dermal dysplasia.

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

Short telomeres may cause symptoms like hair loss and osteoporosis, offering insights into aging.

A point mutation in the androgen receptor gene causes complete androgen insensitivity.

Follicular vitiligo causes hair to gray without skin color loss.

Atrichia with papular lesions causes irreversible hair loss from infancy and is often misdiagnosed.

Early onset baldness in men may indicate a condition similar to PCOS, linked to heart disease, diabetes, and prostate issues.

Cronkhite-Canada syndrome can be diagnosed without gastrointestinal polyps if there is severe mucosal atrophy and edema.