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Hair loss in Cronkhite-Canada syndrome is reversible by treating the gut issues and doesn't need steroid treatment for the hair itself.

Treatment restored normal sexual characteristics and blood condition in a patient with testicular cancer.

A girl with Turner syndrome had psoriasis, alopecia areata, and trachyonychia.

A 63-year-old woman's male-like symptoms were caused by a rare testosterone-producing ovarian tumor, treated by removing her ovaries and fallopian tubes.

A new mutation in the STS gene causes X-linked ichthyosis, even in rare female cases.

A young woman had a rare, aggressive ovarian tumor that was hard to diagnose and treat, leading to disease progression despite treatment.

A woman's severe male hormone excess was caused by a small, hard-to-find ovarian tumor.

A 4-year-old girl has a rare condition causing hairlessness and skin bumps, but normal teeth and sweating.

A new gene mutation causes insulin resistance in a girl and her mother.

A novel CLDN1 mutation in a 2-month-old with NISCH showed improvement with symptom management.

Rapid virilization should be checked for possible ovarian or adrenal cancer.

Popliteal Artery Entrapment Syndrome (PAES) is a rare but possible cause of leg pain during walking, even in untrained women.

Ovarian hyperthecosis caused high testosterone and virilization symptoms in a 60-year-old woman, which improved after surgery.

Accurate diagnosis of progressive supranuclear palsy requires thorough neurological assessments and MRI.

A woman's excess male hormone symptoms were caused by a rare benign tumor in her ovary.

A 5-year-old girl has lipoid proteinosis, causing voice issues, hair thinning, skin lesions, and tongue movement problems.

A 25-year-old man had an unusual case of benign skin tumors and hair loss.

Impaired androgen production in 46,XY DSDs causes ambiguous genitalia and requires long-term care.

A woman developed male characteristics after using unregulated hormone therapy.

Androgens may increase arrhythmias in Brugada Syndrome, while Finasteride could reduce them.

Pseudopelade of Brocq is hard to diagnose and treat, with limited effective options.

Erythromelanosis follicularis faciei can also affect women, though it's rare.

A new genetic change causing early stop in the androgen receptor gene was found in a patient with androgen insensitivity syndrome.

Early detection and biotin treatment improve outcomes for biotinidase deficiency.

Cantú syndrome may be linked to pituitary adenomas.

New ABCA12 gene mutations were linked to a skin condition with scaling and hair loss, and a treatment helped with hair loss in a related case.

Trichothiodystrophy causes unusual hair and developmental issues.