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A postmenopausal woman's hirsutism and high testosterone levels improved after surgery for an ovarian tumor not seen on ultrasound.

The girl has an inflammatory type of scarring hair loss.

Pseudopelade of Brocq is a unique hair loss condition, but its cause and development are still not fully understood.

Congenital triangular alopecia is more common than thought and some treatments can be beneficial for appearance concerns.

A teenage girl had both a rare ovarian tumor and a severe form of polycystic ovarian syndrome.

Non-classic congenital adrenal hyperplasia (NCCAH) can mimic PCOS and requires genetic testing for proper diagnosis and treatment.

FOXN1 duplication can cause excessive hair growth.

Hair loss from hormone therapy in breast cancer patients can be improved with minoxidil treatment.

Adolescents and young adults with Prader-Willi syndrome show a range of sexual interests and behaviors.

No effective treatment exists to stimulate hair growth in atrichia with papular lesions.

Topical minoxidil and hair dye can improve hair density and appearance in congenital hypotrichosis.

Linear Discoid Lupus Erythematosus of the scalp can cause hair loss and should be considered in similar cases.

This rare genetic disorder causes permanent hair loss and skin bumps from birth.

Mutations in the LIPH gene cause woolly hair in a child.

Individuals with this condition often develop male traits and identities at puberty despite being raised as females.

Using buccal mucosa for hypospadias repair in children is effective and reduces complications.

Some breast cancer patients still experience hair loss three years after chemotherapy, especially with taxane-based treatments.

Halo Scalp Ring is a rare newborn hair loss that can be missed, and early diagnosis can avoid extra tests and worry for parents.

Excessive body hair can signal complex health issues.

Treating hyperprolactinemia can help manage PCOS symptoms.

Individuals with male pseudohermaphroditism often do better raised as females with early surgery.

Childhood hypertrichosis is excessive hair growth not linked to hormones, with types based on location and origin.

Genetic testing confirmed a young girl has Atrichia with Papular Lesions due to mutations in the hairless gene.

A 33-year-old woman with PCOS and metabolic syndrome was unusually diagnosed with a bone condition called DISH, suggesting a possible link between these conditions.

The document adds two cases of Gomez-Lopez-Hernandez syndrome and suggests including trigeminal anesthesia and scalp alopecia as key diagnostic criteria.

Some burn patients grew extra hair in areas treated with pressure garments or silicone.

Two sibling goat kids were born with goiter and hair loss.

Micro-CT helps identify suitable areas for surgical procedures based on blood vessel distribution in hypospadias-affected rats.

A mutation in the HOXC13 gene causes hair and nail problems in a Syrian family.