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Bullous pemphigoid, intrahepatic cholangiocarcinoma, and alopecia areata may share immune-related causes.

A patient with steroid sulfatase deficiency had a unique hair pattern and a brain malformation not previously linked to the condition.

A woman with lupus had rare severe symptoms but improved with treatment.

Woolly hair syndrome is a genetic condition causing frizzy, fragile hair.

Chronic lupus and frontal fibrosing alopecia can occur together, but their connection is unclear.

Kallmann syndrome can cause eye issues and other health problems, requiring various treatments.

A patient with a rare chromosome condition also had a rare type of hair loss.

A woman was the first known case to have both polycystic ovary syndrome and autoimmune polyglandular syndrome type 2, suggesting a need to check for both conditions in similar patients.

CARASIL can cause different symptoms even with the same genetic mutation.

A patient with a rare disease had a unique genetic mutation linked to their symptoms.

PCOS requires comprehensive, lifelong care addressing both visible and hidden health issues.

Biotinidase deficiency can mimic neuromyelitis optica and should be considered for accurate diagnosis and treatment.

Dystonia may be part of PAS-4 and linked to immune issues.

Consider Castleman's disease in similar cases; histology and steroids help diagnose and manage it.

Females are more affected by immune-related skin diseases, needing targeted health interventions.

Early detection of Graham-Little-Piccardi-Lasseur syndrome is key for better management.

Multiple eye conditions were studied, highlighting the importance of various imaging methods for diagnosis, the vision side effects of drugs tamoxifen and Propecia, and the usefulness of optical coherence tomography for diagnosing and monitoring macular and retinal diseases.

Rothmund-Thomson syndrome type 2 can cause chronic, poorly healing wounds.

The MBTPS2 gene variant c.970+5G>A is a common mutation causing IFAP syndrome.

A 21-year-old male with a rare genetic disorder experienced sudden hair loss and high DHEAS levels, likely due to a condition similar to PCOS, usually seen in women.

The study concludes that Loose Anagen Hair Syndrome is a benign condition that usually improves with age but can be hard to diagnose and stressful for the family.

An 18-year-old man was diagnosed with a rare genetic disorder causing hair loss, severe light sensitivity, and skin issues.

A woman's severe male-like symptoms were caused by a rare, benign tumor in her ovary that produced male hormones.

A family showed a new condition with inherited hair loss and skin changes, possibly due to one genetic disorder.

Trichotillomania can cause severe complications like hairballs in the stomach, needing surgery and psychiatric care.

Consider NF1 in newborns with rare congenital anomalies.

A patient had both chronic lupus and systemic scleroderma, requiring careful treatment to manage symptoms.

A strict gluten-free diet can improve liver issues in celiac disease.

COVID-19 vaccination may be linked to MIS-C in children, highlighting the need for quick diagnosis and treatment.

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