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A woman with X-linked chronic granulomatous disease developed lupus-like skin lesions, improved with treatment, suggesting a unique skin condition in carriers.

Black women with CCCA are more likely to have uterine fibroids.

A girl with hereditary chorea, likely Huntington's disease, had her condition worsened by lupus.

Truncating mutations in the C2orf37 gene cause Woodhouse–Sakati syndrome.

A woman with lupus and severe nerve damage improved with specific treatments.

Chronic cutaneous lupus erythematosus causes scarring, hair loss, and skin discoloration, especially on sun-exposed areas.

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

The clinical signs of Adams-Oliver syndrome can vary greatly, even among family members.

Genetic factors, especially PADI3 gene variants, contribute to CCCA in women of African descent.

Autosomal recessive woolly hair is rare and involves tightly coiled hair without other health issues.

Two rare bald spots on the back of the scalp were found to be lupus, not alopecia areata.

Untreated congenital adrenal hyperplasia can lead to complications like stroke and needs glucocorticoid treatment.

Leukemia can sometimes appear as unusual skin issues in children.

A rare genetic mutation causes Woodhouse-Sakati syndrome symptoms.

A woman with discoid lupus improved with treatment after being misdiagnosed with a different hair loss condition.

CCCA is a scarring hair disorder mainly affecting people of African descent, needing better awareness and treatment.

Hair evaluation is crucial for early diagnosis and management of ARCI, as hair loss often indicates severity.

Most patients with Cutaneous Lupus Erythematosus are young females, and dermatologists play a key role in diagnosis.

CCCA mainly affects Black women and is linked to high-tension hairstyles, heating tools, chemical relaxants, and genetics.

Patients with a specific genetic variant have more severe alopecia areata and higher recurrence rates.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

Consider systemic lupus erythematosus in patients with unexplained intracranial hypertension.

Alopecia areata patients are more likely to develop systemic lupus erythematosus.

Cutaneous lupus erythematosus is a common skin condition in lupus, affecting mostly young adult females.

A 38-year-old man was diagnosed late with Kearns-Sayre syndrome after being wrongly treated for epilepsy.

Researchers found two new genetic variants linked to Alzheimer's disease.

Visceral leishmaniasis can mimic rheumatoid arthritis symptoms, especially in immunocompromised patients.

About 8% of people with systemic lupus erythematosus have chronic scarring alopecia, with certain symptoms and positive antibodies increasing the risk, while immunosuppressants may lower it.

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

A young woman with visual issues and other symptoms was diagnosed with lupus and antiphospholipid syndrome, and improved with treatment.