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A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.

A rare case of lupus linked to thymoma shows complex diagnosis and management challenges.

Some immunosuppressed patients can get unusual skin infections from Malassezia, which can be treated with antifungal medication.

Some families have a genetic condition where they are born with irregular scalp defects.

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

Superficial granulomatous pyoderma is a unique, mild form of skin disease that often heals without strong medication and responds well to milder treatments.

Variants in the CCDC47 gene are linked to trichohepatoneurodevelopmental syndrome.

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

People with anhidrotic ectodermal dysplasia may get severe bronchitis if exposed to dust.

A 21-month-old boy has a rare genetic disorder causing sparse hair due to an LSS gene mutation.

Mixed Connective Tissue Disease can develop from overlapping symptoms of several autoimmune diseases, making diagnosis complex.

Some patients with mycosis fungoides or Sézary syndrome experience hair loss, which may be similar to alopecia areata or linked to skin lesions, possibly due to abnormal T cells, and bexarotene can help treat it.

Thymoma may link myasthenia gravis, nail dystrophy, and alopecia areata.

Cantu syndrome, which causes excessive hair growth and skin issues, is due to a mutation in the ABCC9 gene, and understanding this could help develop new treatments for hair diseases.

A CCS patient with severe complications was successfully treated using combined therapies.

A 6-year-old girl was diagnosed with a rare hair disorder and started treatment with topical minoxidil.

Early diagnosis of leprosy is crucial to prevent disabilities and spread, even in non-endemic areas.

Most people with metabolic syndrome in Brazil have skin issues, especially if they are morbidly obese.

Brunsting-Perry pemphigoid can cause scarring hair loss and may be underdiagnosed.

A woman with myotonic dystrophy had multiple skin tumors on her scalp, suggesting a genetic link.

JetPeel-assisted minoxidil improves hair density and thickness more than minoxidil alone.

A woman with skin and joint issues progressed from one type of lupus to another, highlighting the need to recognize complex conditions.

A 13-year-old boy with Cushing syndrome has high cortisol levels from a pituitary gland issue and underdeveloped sexual characteristics.

Early diagnosis of pseudopelade of Brocq in men is crucial to prevent permanent hair loss.

Abnormal T-cells from thymomas cause non-motor symptoms in some myasthenia gravis patients.

A 14-year-old girl with Loose Anagen Hair Syndrome was successfully treated with oral Minoxidil and a Silicon supplement.

Neuroendocrine paraneoplastic syndromes often show skin changes, helping early diagnosis and requiring a team approach for best care.

Trichothiodystrophy causes unusual hair and developmental issues.

The boy's symptoms improved with vitamin C treatment, highlighting the need to consider scurvy in kids with unusual diets.

Hair loss in Cronkhite-Canada syndrome may be due to an autoimmune response.