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Older men's scalp damage increases with age and sun exposure, a baby girl in the Philippines has Schimmelpenning syndrome, and thyroid screening is advised for children with hair loss and certain risk factors.

Non-coding RNAs may be key in diagnosing and treating rare skin disorders.

HtrA2 activity is crucial for normal hair growth by regulating fat cell development.

The nodule was a benign cutaneous lymphadenoma, not cancer, and was successfully removed.

The report described a unique case of Cronkhite-Canada syndrome with unusual polyps and an association with multiple myeloma.

Porokeratotic eccrine and hair follicle nevus is a very rare skin disorder possibly caused by a GJB2 gene mutation.

The boy's hair and skin color differences are due to a pigmentation disorder.

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

Mutations in the WNT10A gene cause Short Anagen Hair syndrome and increase the risk of male pattern hair loss.

A 16-year-old boy had a rare case of Becker's nevus on his face and mouth.

Cystic panfolliculoma is a rare, harmless tumor that can be confused with other skin tumors.

Researchers found a way to make rat hair follicle cells start turning into motor neuron-like cells, but couldn't fully turn them into working motor neurons.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

Neuroendocrine paraneoplastic syndromes often show skin changes, helping early diagnosis and requiring a team approach for best care.

RSPO1 mutations in certain patients lead to skin cells that don't develop properly and are more likely to become invasive, increasing the risk of skin cancer.

Seborrheic keratoses may partly come from hair follicle cells.

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

A woman's chronic head pain after hair transplant surgery was cured by removing a post-traumatic neuroma.

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

The neck mass was a rare benign "wattle," surgically removed for diagnosis and appearance.

Trichostasis spinulosa can be diagnosed with a simple skin biopsy and treated with specific gels, but lesions may return after stopping treatment.

A man had rare skin tumors with bone formation and cholesterol deposits.

A woman's hair loss improved after removing a tumor in her thymus gland, suggesting hair loss can be linked to such tumors even without a specific muscle weakness condition.

The early genes of a specific virus can cause abnormal skin cell growth and hair follicle changes.

Certain types of mucopolysaccharidoses cause significant hair abnormalities.

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

A 29-year-old man had a jaw plaque diagnosed as follicular mucinosis, linked to nestin-positive hair follicle stem cells.

Keratin 15 cells from hair follicles help develop and maintain skin tumors in mice.

A young woman had a rare scalp tumor usually found in older women.

A woman with hair loss had a benign sweat duct tumor found during a scalp biopsy.