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Temporal triangular alopecia causes permanent hair loss and can be managed with treatments like minoxidil or hair transplantation.

A rare genetic mutation caused severe symptoms in a 6-year-old girl with mandibuloacral dysplasia type A.

The report shows that a rare benign tumor was successfully removed from inside the mouth to avoid scarring on the face.

Combining medication and minimally invasive techniques can effectively manage Marine-Lenhart syndrome.

Early diagnosis and hormone therapy can significantly improve outcomes for post-partum pituitary insufficiency in resource-limited settings.

A new DSG4 gene mutation causes hair defects in a young girl.

Rare ovarian tumors can cause hyperandrogenism, even if imaging appears normal.

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

A girl had two rare hair conditions that helped understand their overlap.

A 6-year-old girl was diagnosed with a rare hair disorder and started treatment with topical minoxidil.

New therapies for Birt–Hogg–Dubé syndrome are being developed based on understanding the FLCN gene's role.

A rare skin condition appeared on a 19-year-old woman's scalp.

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

A 15-year-old girl with no menstrual period was diagnosed with a genetic condition that makes her body unable to respond to male hormones, leading to female characteristics despite having male genetic makeup.

Children with partial biotinidase deficiency are healthy at birth but may develop symptoms that improve with biotin therapy.

A woman's scalp nodule was a common, harmless pilar cyst, treated by surgical removal.

A six-year-old girl has early signs of puberty, needs no treatment, but requires regular check-ups for future health risks.

Hair matrix cysts are rare skin nodules with unique features, often needing surgical removal.

A truncated protein linked to breast cancer may change cell adhesion.

The document suggests that certain protein deficiencies and scalp blistering in Epidermolysis Bullosa may cause hair loss.

A 6-year-old Asian boy has a rare scalp condition causing hair loss and thickening, with unclear causes and no effective treatment.

A 7-year-old girl had a non-painful skin growth at her belly button, which was removed and identified as a keratinous cyst.

Hedgehog signaling controls hair follicle development and can affect skin cancer growth.

A 15-year-old girl with missed periods was diagnosed with a pituitary disorder and treated with hormones and steroids.

The woman was diagnosed with lichen sclerosus, a rare skin condition, after initial misdiagnosis and ineffective treatments.

Isotretinoin may effectively treat hereditary hypotrichosis simplex, a rare hair loss condition.

Long-term repeated cupping therapy can cause unexpected localized hair growth.

Sheehan syndrome can cause hormone deficiencies after childbirth, but treatment can improve symptoms.

A woman's high testosterone and related symptoms were caused by overactive cells in her ovaries.

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