Search

everythinglearnresearchcommunity

for

Search:↓

Trichoscopy is useful for diagnosing and monitoring systemic lupus erythematosus, with certain hair and scalp changes indicating more active disease.

Dermoscopy helps diagnose and monitor treatment for hair loss from scarring conditions like discoid lupus and lichen planopilaris.

Chronic scarring alopecia is common in SLE patients and needs early detection and management.

Satoyoshi syndrome is likely an autoimmune disease that mainly affects young women and improves with immune-related treatments.

Graham-Little syndrome causes hair loss and skin bumps, with difficult treatment options.

A new genetic mutation in the TRPS1 gene causes Trichorhinophalangeal Syndrome, leading to specific hair, dental, and bone issues.

Parental socioeconomic status doesn't improve dietary habits or reduce disease severity in children with sickle cell disease.

The patient with EEC syndrome had scarring alopecia due to deep folliculitis, possibly linked to abnormal hair structure.

The modified Crawford technique resulted in less lagophthalmos and better cosmetic outcomes for patients with lateral droop.

Ossification in trichilemmal cysts is more common than previously believed.

Hair transplantation in nevus sebaceus maintains hair cycling but doesn't prevent tumor growth; complete excision is recommended.

Women with PCOS have distinct retinal changes compared to healthy women.

A woman with lupus had right heart failure due to blood clots in her lungs, but treatment improved her condition.

Segmental vitiligo affects hair follicle melanocytes, causing small, uniform depigmented spots.

Early recognition and treatment of EPDS are crucial to prevent permanent hair loss.

Soft-tissue calcification is rare in systemic lupus erythematosus.

Genetic analysis is crucial for diagnosing ectodermal dysplasia syndromes, and new therapies may help improve skin issues.

Anti-phospholipid antibodies in SLE can cause thrombosis and bone necrosis.

ZNF750 and MPZL3 are important in causing seborrheic dermatitis.

Timely diagnosis of SLE is crucial due to symptom overlap with fibromyalgia.

A rare dual diagnosis of alopecia areata and lichen planopilaris requires thorough evaluation for effective treatment.

The document concludes that detailed clinical descriptions of seven family cases help understand dominant dystrophic epidermolysis bullosa's symptoms and inheritance.

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

A new mutation in the mitochondrial DNA was found in a boy with MELAS, even though his family didn't show typical signs.

SLE can increase the risk of blood clots, leading to heart failure, but treatment can improve heart function.

People with alopecia areata have similar retinal structures but thicker choroidal regions compared to those without the condition.

Visual field defects in lupus nephritis can be caused by hypertensive retinopathy, not glaucoma or medication toxicity.

The PER3 rs772027021 SNP may cause mild skin pigmentation changes in a new subtype of dyschromatosis universalis hereditaria.

A person with Turner Syndrome showed severe schizophrenia that didn't respond to treatment and had brain shrinkage.