Search

everythinglearnresearchcommunity

for

Search:↓

Anorexia Nervosa and Bulimia Nervosa are complex eating disorders with increasing incidence among young females, significant morbidity, and varying mortality rates, requiring more research for better treatment.

A woman with dermatomyositis improved after treatment for neck panniculitis, suggesting similar treatment for related conditions.

The NIPAL4 mutation c.527C>A is common in Romanian patients with autosomal recessive congenital ichthyosis.

The girl has a genetic hair condition causing thin hair since childhood.

Rituximab may be an effective treatment for Cronkhite-Canada syndrome with kidney disease.

A Gsdma3 mutation causes hair loss due to stem cell damage from skin inflammation.

A Chinese male with a new genetic mutation has a skin condition and severe urinary issues, with treatments having mixed success.

Cladribine has known risks and potential new safety concerns, requiring careful monitoring.

The mK6irs1/Krt2-6g gene likely causes wavy hair in mice.

Biotinidase deficiency has various symptoms and can be treated with biotin supplements.

Two boys had a rare skin condition needing to be differentiated from similar disorders, with unclear inheritance due to few cases.

Mogamulizumab, a skin cancer drug, may cause hair loss similar to alopecia areata.

Tunisian children with hereditary vitamin D-resistant rickets showed improvement with calcium treatment, and new genetic mutations were identified.

The RAS pathway affects hair growth differently in CFCS and CS.

A mutation in the FAM83G gene is linked to skin and hair abnormalities in two related individuals.

A hereditary condition causes hair loss and twisted hair in some family members.

The document reports a unique case of woolly hair with a combination of conditions not previously seen together.

Targeting ornithine decarboxylase can help prevent skin cancer.

Kainar syndrome symptoms may be linked to nuclear test exposure effects.

The AMHR2-482A>G gene change is linked to higher PCOS risk.

Epidermolysis bullosa in calves was not caused by mutations in the keratin genes bKRT5 and bKRT14.

The patient improved with treatment for depilating folliculitis.

DNA methylation changes are linked to skin diseases with inflammation.

"Moth-eaten alopecia" can be a sign of secondary syphilis, treatable with penicillin.

A man with Cronkhite-Canada syndrome improved significantly with immunosuppressive therapy.

A family had a genetic condition causing hair loss on the scalp, passed down through four generations.

Two siblings had a rare immune disorder caused by a FOXN1 gene mutation.

Mixed Connective Tissue Disease can develop from overlapping symptoms of several autoimmune diseases, making diagnosis complex.

La detección temprana y precisa de la pseudopelada de Brocq es crucial para detener su progresión.