Search

everythinglearnresearchcommunity

for

Search:↓

Pegylated interferon-alpha 2a can cause a rare nerve disorder, but early treatment can lead to full recovery.

Identical twins both had a rare hair loss condition, suggesting it might be genetic.

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.

The Pfizer COVID-19 vaccine may rarely trigger nail psoriasis.

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

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

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

A 3-year-old girl has a rare condition causing sparse hair and nail issues, with minimal improvement from treatment.

HPV-150 and HPV-151 are rare skin viruses linked to warts and some skin cancers.

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.

A 4-year-old girl has a rare condition causing hairlessness and skin bumps, but normal teeth and sweating.

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.

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

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