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A new genetic mutation causes severe Leydig cell hypoplasia, affecting sexual development.

A 12-year-old boy with a rare genetic condition has progressive hair loss with no effective treatment.

An 18-year-old girl was diagnosed with a rare hereditary hair loss condition, despite no family history.

An 8-year-old girl has a rare genetic disorder causing complete, irreversible hair loss and skin bumps.

A rare skin growth in a baby was successfully removed without coming back.

The patient has a rare skin condition that shows features of two known disorders.

A rare, harmless hair condition was found in an infant's eyebrow, needing no treatment.

Zinc supplements and weaning cured a breast-fed baby's zinc deficiency caused by a gene mutation.

Gynecomastia and premature thelarche often resolve naturally but need evaluation to rule out serious issues.

Hyperthyroidism can hide signs of high androgen levels in females.

Early recognition of skin lesions in Birt-Hogg-Dubé syndrome is crucial for detecting renal tumors early.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

Becker's Nevus Syndrome is a rare condition with a skin patch and possible bone and muscle abnormalities, treated mainly for appearance.

A man with kidney tumors and lung cysts was diagnosed with Birt–Hogg–Dubé syndrome and treated successfully, with genetic testing confirming the diagnosis.

Congenital atrichia with papular lesions causes permanent hair loss and skin bumps from birth.

A hairless patch on a boy's scalp from birth injury improved with minoxidil treatment.

A baby had a unique skin condition with a pale patch and surrounding dark hairs, not linked to other health issues.

Researchers found a gene mutation responsible for a rare hair loss condition.

Polythelia pilosa is a type of extra breast tissue with hair and should be classified as such.

Thymic LCH may be underdiagnosed, so thymic ultrasound should be considered in infants with cutaneous LCH.

A five-year-old girl has a harmless, unchanging bald patch on her scalp.

The young woman has a benign, hereditary skin condition with no signs of a more serious syndrome.

The infant's hair loss resolved naturally by 20 months without treatment.

A patient with untreated congenital adrenal hyperplasia had large benign tumors in her adrenal glands removed, improving her symptoms.

A hereditary condition causes hair loss and twisted hair in some family members.

A rare skin condition with cysts was found on a 5-year-old boy's scalp.

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

Oral minoxidil and growth factors improved hair density and thickness in a girl with hereditary hair loss.

An 11-year-old girl with hair thinning was diagnosed with monilethrix and early androgenetic alopecia.

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