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Lupus affects the body and skin, causing joint pain and skin issues that can be treated with steroids and antimalarial drugs.

A child with skin and tooth symptoms was found to have a genetic mutation causing cardiocutaneous syndrome, leading to heart problems.

Psychosis can be an early sign of neuropsychiatric lupus, treatable with tailored medication.

A patient with Myotonic dystrophy type 1 had multiple tongue hemangiomas and was sensitive to anesthesia.

SLE patients in eastern Saudi Arabia have a generally good prognosis despite multi-organ involvement.

Early recognition and multidisciplinary management of Whitaker syndrome can improve patient outcomes.

A rash from semaglutide may be due to propylene glycol, not the drug itself.

Enzyme replacement therapy improved multiple symptoms of homocystinuria in mice.

People with Myotonic Dystrophy type 1 are more likely to have certain skin conditions, but not more likely to get skin cancer.

A 73-year-old woman with Hypopigmented Mycosis Fungoides, a rare skin lymphoma, experienced disease progression despite treatment, emphasizing the need for ongoing monitoring.

A possible link exists between hair follicle abnormalities, hair loss, and muscle weakness.

People with Fibromyalgia Syndrome often have skin symptoms, which can worsen their quality of life and increase depression.

Lupus enteritis is a rare but serious gut inflammation in lupus patients, often hard to diagnose without prior lupus symptoms.

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

Chronic scalp lesions with crusts and pus indicate Erosive Pustular Dermatosis, which is confirmed by biopsy and effectively treated with strong topical steroids.

The conclusion suggests that managing antioxidant levels and the calcium to magnesium ratio may help address Long Covid and related chronic fatigue conditions.

GERD symptoms are linked to acid exposure time and daytime sleepiness, influenced by ghrelin levels.

Trichoscopy can help diagnose and assess disease activity in connective tissue diseases by identifying specific hair and scalp signs.

A 37-year-old male with severe skin and internal issues has a rare inherited skin condition called dystrophic epidermolysis bullosa.

Improving mitochondrial health may help alleviate symptoms like chronic fatigue and depression.

Effective treatment improved skin and overall symptoms in a lupus patient.

Epidermolytic ichthyosis can be inherited in a semidominant way with mild symptoms in carriers.

Dermatologists should consider alpha-gal syndrome in patients with unexplained chronic skin issues.

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

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

Early and accurate diagnosis of congenital smooth muscle hamartomas is crucial to distinguish them from other conditions.

Hyperaesthetic leucotrichia in horses causes painful, recurring skin lesions and hair color changes, especially in Arabian and American paint horses.

The twins' condition is unique and doesn't match any known syndromes.

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