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The brothers have congenital ichthyosis, and the older brother's eye issues are due to different genetic mutations.

Olmsted syndrome is a rare skin disorder causing thickened skin and other symptoms.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

Long COVID affects many survivors with ongoing symptoms, needing more research and care.

A multidisciplinary approach is crucial for treating complex cases of Rapunzel syndrome in children.

A young woman with late-stage Vogt-Koyanagi-Harada disease was successfully treated at a hospital.

Oral Acitretin effectively resolved symptoms in a child with Netherton syndrome.

A 72-year-old man was diagnosed with a rare skin form of Rosai-Dorfman disease after years of misdiagnosis.

A 22-year-old with multiple autoimmune diseases needs a multidisciplinary treatment approach.

A new mutation in the hHb1 keratin gene is linked to the hair disorder monilethrix.

Netherton syndrome causes skin and hair issues, confirmed by "bamboo hair" under dermoscopy, with no cure but managed with topical treatments.

COVID-19 can lead to different skin symptoms and might trigger autoimmune diseases in genetically susceptible people.

A deficiency in the TTC7A gene causes immune problems, gut issues, and hair loss.

Congenital atrichia with papular lesions is often misdiagnosed, and new diagnostic criteria can improve accuracy.

Chronic kidney disease can cause skin problems that affect patient quality of life, and treating these conditions can improve outcomes.

COVID-19 may trigger systemic lupus erythematosus, requiring careful diagnosis and treatment.

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

More research is needed to understand sex and racial differences in long COVID.

Syphilis can mimic other diseases, making diagnosis challenging, but proper testing and treatment are effective.

A new rat strain with a specific gene mutation causes hair loss and kidney issues.

Two patients treated with TAC for mouth fibrosis improved but developed Cushing's Syndrome symptoms.

The boy likely has a fungal infection causing hair loss.

Advancements in understanding, diagnosing, and managing congenital adrenal hyperplasia have improved treatment and long-term outcomes.

Hepatitis C and alcohol abuse may lead to porphyria cutanea tarda.

Trichothiodystrophy causes abnormal protein deposits and distortion in hair follicles.

Cupric chloride treatment corrected abnormal Purkinje cell development in brindled mice.

Graham-Little syndrome causes scarring hair loss and skin bumps.

A chest X-ray can effectively diagnose ectopic ACTH secretion from lung tumors.

An infant with Hutchinson-Gilford Progeria Syndrome had successful surgery to fix breathing issues caused by a new genetic mutation.

Trichoscopy helps accurately diagnose Netherton syndrome, often mistaken for atopic dermatitis.