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Mutations in the LSS gene cause a rare type of hereditary hair loss.

A 93-year-old woman developed a rare scalp condition after therapy, which improved with steroids, not antibiotics.

A woman with breast cancer developed a rare condition causing excessive fine hair growth on her face and body.

A woman with dermatomyositis showed rare skin symptoms, was treated successfully, and her case suggests checking for cancer in similar patients.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

Erosive pustular dermatosis is a rare skin disease that's hard to treat and affects the scalp or legs.

Congenital Triangular Alopecia is a rare, non-scarring hair loss that can be surgically treated in females for cosmetic reasons.

Congenital alopecia in domestic animals is rare and involves abnormal hair follicle development, needing better understanding and classification.

SACUMAN, a rare condition causing hair loss without clear signs, is often misdiagnosed and needs scalp biopsies for accurate detection.

Fibrodysplasia ossificans progressiva is a rare genetic disorder that causes extra bone growth and symptoms of premature aging.

Some stem cells in the body rarely divide, which could help create better treatments for diseases and aging.

Allergic reactions to blood thinners are rare but can be serious, requiring careful management and alternative treatments.

Three white adults had a rare scalp condition with increased fat and sometimes hair loss, suggesting it's not limited to black women and might be more widespread.

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

Toxic Epidermal Necrolysis is a rare, serious skin condition that can affect anyone, is more common in women, and may be linked to genetics, with a 20% mortality rate mainly due to sepsis.

A woman with cervical cancer had rare scalp metastasis causing a unique type of hair loss.

Children with severe ichthyosis and growth failure rarely have nutritional deficiencies or gastrointestinal issues, but may experience chronic dehydration.

There is no standard treatment for the rare Cronkhite–Canada syndrome, which can be fatal and lead to cancer.

A young woman with a rare hair loss condition improved with steroid and biotin treatment.

A 3-year-old boy had a rare hairball condition usually seen in teenage girls.

A 66-year-old man with a rare case of male frontal fibrosing alopecia did not regrow hair despite treatment.

A 2-year-old boy with a rare brain malformation may have Gomez–López-Hernández syndrome.

Fragile hair in children is rarely linked to trichothiodystrophy (TTD).

Lichen Planopilaris in teens is rare, often misdiagnosed, and responds well to steroids.

Hair loss from alopecia areata can rarely be caused by dental problems, and treating the dental issue may reverse the hair loss.

Mutations in the NR3C1 gene cause a rare condition that affects hormone signaling and can lead to various symptoms, with dexamethasone as a treatment option.

Hair tourniquet syndrome is a rare condition where hair wraps around an infant's body part, needing quick removal to prevent damage.

Eruptive vellus hair cysts are rare, benign skin lesions that are hard to treat.

An 84-year-old man got a rare scalp condition from using imiquimod cream, which was cured with systemic steroids.

A young woman had a rare skin reaction to a medication for her joint disease, and a combination therapy improved her condition.