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LTBP1 is a key regulator in diseases and a potential target for new treatments.

Metreleptin treatment significantly improved metabolic health in a boy with congenital generalized lipodystrophy.

In Italian patients with lupus, the most common skin issue was chronic cutaneous lupus, especially discoid lesions, and nonspecific skin problems occurred in about a third of those with systemic lupus, mainly during active disease.

Birt–Hogg–Dubé Syndrome requires genetic testing for accurate diagnosis due to its similarities with tuberous sclerosis.

Early and aggressive treatment with individualized care plans is crucial for managing pediatric systemic lupus erythematosus.

ILC1-like cells can cause alopecia areata by themselves.

Discoid Lupus Erythematosus is more common in women aged 31-40, often worsened by sunlight, and confirmed by specific lab tests.

PNH can occur in patients with SLE, so doctors should be aware of this.

Trans-esophageal echocardiography is crucial for accurately diagnosing heart issues in lupus patients.

Recognizing rare causes of MASLD is crucial for effective treatment and preventing complications.

The newborn was diagnosed with a rare skin disorder causing blisters, which requires careful wound care and family support.

A woman with both TLE and SLE improved with hydroxychloroquine treatment.

A rare autoimmune disease caused the woman's scalp blisters and hair loss, successfully treated with medication.

LDE225 is a promising skin-applied treatment for basal cell carcinoma with good skin penetration and effectiveness.

Black patients with discoid lupus erythematosus have more severe skin damage and higher chances of dyspigmentation, scalp, and ear involvement.

Recognizing lupus as a cause of severe gut issues is crucial for effective treatment.

Lichen simplex chronicus on the scalp can be diagnosed by specific hair and skin signs and treated with corticosteroids and therapy.

Protein-losing enteropathy worsened with lupus symptoms but improved with prednisolone.

The study found two new mutations in a Chinese patient with severe biotinidase deficiency.

The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

The decision board effectively helps lupus nephritis patients in Brazil choose treatments by clearly presenting options and side effects.

Most pregnancies with SLE resulted in intrauterine growth restriction (IUGR).

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

DDS treatment for LABD can cause severe side effects like anemia and hair loss, requiring careful monitoring.

Scalp skin condition LEDS has similar features to Zoon's balanitis, a mucosal skin disorder.

A man with kidney tumors and lung cysts was diagnosed with Birt–Hogg–Dubé syndrome and treated successfully, with genetic testing confirming the diagnosis.

Buserelin safely and effectively suppresses early puberty, potentially improving final height.

The document suggests that severe hair loss in SLE patients may be an early sign of scalp DLE, treatable with immunosuppressive therapy.

Squaric acid dibutylester for alopecia areata can cause benign skin lymphoid growths.

Alopecia in patients with epidermolysis bullosa varies in severity and is often caused by skin blistering or trauma.