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The study found that Central Centrifugal Cicatricial Alopecia mainly affects middle-aged African descent women, is linked to certain hair care practices and genetics, and often goes undiagnosed for years.

A 2-year-old girl had a hair disorder not shared by her identical twin.

A 16-year-old boy with Castleman's disease and lupus was successfully treated and showed no recurrence.

Differentiating PCOS from NCAH helps improve diagnosis and treatment.

Satoyoshi Syndrome is hard to diagnose and treat due to its rarity and complex symptoms.

Stopping birth control pills may have triggered a manic episode in a woman with HAIR-AN syndrome.

ODC1 gene mutations cause a neurodevelopmental disorder with large head size, hair loss, and facial abnormalities.

A rare case of Cushing syndrome was successfully treated with one-sided adrenal gland removal, suggesting personalized treatment is important.

Connexin-26 gene mutations may increase cancer risk in KID syndrome patients.

A complex X chromosome rearrangement can increase the risk of multiple autoimmune diseases.

Netherton's syndrome may have a familial link and doesn't always include atopy.

One twin girl has Loose anagen syndrome with poorly anchored hair, diagnosed with a simple hair pull test, while her identical twin does not have the condition.

Nonclassic congenital adrenal hyperplasia is a common genetic disorder that can cause a range of symptoms and requires personalized treatment.

CRPS type I is a complex pain condition with no proven cure, requiring personalized treatment.

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

Cantu syndrome, which causes excessive hair growth and skin issues, is due to a mutation in the ABCC9 gene, and understanding this could help develop new treatments for hair diseases.

Primary cicatricial alopecia is linked to various health issues, indicating broader systemic problems.

Ellis van Creveld syndrome, a rare genetic disorder, can cause unexpected abnormalities in various body organs, requiring thorough patient evaluations.

Corneodesmosin is essential for skin and hair health, and its dysfunction can lead to skin and hair disorders.

Woodhouse-Sakati syndrome can cause writer's cramp and other varied symptoms, highlighting the importance of genetic testing for diagnosis.

Cabergoline helped a boy with Cushing disease get better after surgery and radiotherapy didn't work.

Recognizing CVG can help diagnose systemic amyloidosis early.

Adrenocortical carcinoma is a rare, aggressive adrenal gland cancer with a poor outlook.

Congenital Adrenal Hyperplasia is a rare inherited disease causing hormone imbalances, affecting growth, fertility, and heart health, diagnosed through blood tests and treated with medication and lifestyle changes.

NISCH syndrome is a rare genetic disorder affecting skin and liver, with variable symptoms and limited treatment options.

A rare case of severe scalp hair loss and nail issues in keratosis follicularis was observed.

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

A girl had two rare hair conditions that helped understand their overlap.

A woman with myotonic dystrophy had multiple skin tumors on her scalp, suggesting a genetic link.

Woodhouse-Sakati syndrome often causes sexual development issues, hair loss, learning disabilities, deafness, muscle contractions, limb pain, and diabetes.