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Early diagnosis of PSIS can lead to normal height with growth hormone and testosterone treatment.

Recognizing macro-TSH is crucial to avoid unnecessary treatments.

A 2-year-old boy has a rare hair disorder causing brittle hair and hair loss, which may improve with age.

A baby was diagnosed with IFAP syndrome due to a new genetic mutation, showing severe skin and developmental issues.

Hair examination helps diagnose rare neurological diseases in children.

Steroid cell tumors in the ovary are rare, can produce testosterone causing symptoms, and are mainly treated with surgery.

Half-siblings with a rare skin condition improved with treatment for a fungal infection, but hair loss remained.

Woolly hair syndrome is a genetic condition causing frizzy, fragile hair.

A toddler with a rare adrenal gland tumor causing male-like physical changes was successfully treated with surgery.

Thyroid storm is hard to diagnose due to vague symptoms but needs urgent attention.

Managing rare genetic diseases like osteogenesis imperfecta and Escobar syndrome is complex and requires both medical and surgical treatments.

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

Tislelizumab can cause cutaneous lupus erythematosus.

Timely surgery successfully repaired a boy's penis after a hair caused severe damage.

Congenital triangular alopecia is a hair loss condition present from birth or early childhood with no effective treatment needed.

Forehead taping can sometimes lead to unexpected problems.

Tofacitinib effectively treated severe alopecia areata in a 14-year-old girl.

Trichoscopy helped diagnose and treat a child's fungal scalp infection by spotting specific hair shapes.

Tofacitinib treatment is used for teenagers with alopecia areata.

Autoimmune conditions can be linked to trichoepitheliomas, with treatment focusing on cosmetic concerns.

Anti-TNF therapy can cause a rare hair loss condition similar to alopecia areata.

A new genetic mutation was found causing hair and eye issues in a boy.

The patient had a severe itchy rash and hair loss in the armpits.

People with autism are more likely to develop alopecia areata than those without autism.

People with keratosis pilaris might be more likely to get a rare type of tinea versicolor.

Hyperthyroidism can hide signs of high androgen levels in females.

A Japanese patient with a rare genetic disorder had a less severe case than others, suggesting other factors may affect symptoms.

The report shows a young man with Hutchinson-Gilford Progeria Syndrome had typical and additional eye problems related to the disease.

Inhaled steroids in children may cause excessive hair growth and not always go away after stopping the medication.

EGFR inhibitors can cause unusual localized hair growth.