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Treatment with prednisolone and dapsone stopped new blisters and partially healed previous ones.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

The Korean study found that twenty-nail dystrophy mainly affects adults, more often women, and has five distinct types with different clinical progressions.

MSUD patients need careful monitoring of amino acids and zinc to prevent severe symptoms.

Tay syndrome is a unique genetic disorder causing skin, hair, and developmental issues.

A woman with both Cronkhite-Canada syndrome and myelodysplastic syndrome improved significantly with corticosteroid treatment.

A patient with "strawberry gingivitis" improved after correct treatment for Granulomatosis with polyangiitis, highlighting the need for early diagnosis.

The study created a mouse model that survives longer and shows fewer symptoms of pemphigus vulgaris.

Autoimmune Polyendocrine Syndromes involve specific combinations of endocrine and non-endocrine autoimmune diseases.

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

Two siblings with a rare type of rickets and hair loss had low vitamin D levels, which is not typical for their condition.

A 30-year-old man with rare skin conditions improved with antibiotics and surgery, hinting at a link to rosacea.

The study concludes that Twenty-nail dystrophy is more common in boys among children and in women among adults, with varying response to treatment.

A young woman with late-stage Vogt-Koyanagi-Harada disease was successfully treated at a hospital.

A boy with chromosome 13q deletion syndrome developed eye cancer, a woman with breast cancer lost vision due to a rare side-effect of her treatment, a man's vision worsened after using a hair loss drug, and two rare disorders were discussed. Optical Coherence Tomography is useful for diagnosing and monitoring these conditions.

Impaired androgen production in 46,XY DSDs causes ambiguous genitalia and requires long-term care.

Discoid Lupus Erythematosus often causes scarring hair loss, is influenced by genetics and environment, and requires early treatment to prevent worsening.

A genetic mutation caused severe rickets and alopecia in an Indian patient, but high-dose calcium and phosphate treatment improved their condition.

The document reports a rare case of ECCL with a new association with optic disc colobomas.

Hair thinning and loss in a girl with a rare metabolic disorder was linked to her condition.

Discoid lupus erythematosus can be mistaken for a skin infection, complicating diagnosis and treatment.

Improved nutrition quickly healed the patient's skin lesions.

A girl with type 1 diabetes developed a serious eye condition very early, suggesting the need for earlier eye checks and that early treatment can work well.

Digital gangrene can be an initial symptom of late-onset systemic lupus erythematosus.

The hair disorder was caused by abnormal protein formation, making hair easily damaged.

Pyoderma gangrenosum can occur in rheumatoid arthritis patients and may be mistaken for vasculitis.

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.

A 50-year-old woman with breast cancer developed an autoimmune skin disorder, highlighting the need for thorough checks and team-based treatment.

A man with a weakened immune system was diagnosed with a rare skin condition called trichodysplasia spinulosa using skin examination techniques.