Search

everythinglearnresearchcommunity

for

Search:↓

A man with a rare skin condition and a new gene mutation developed high calcium levels due to his treatment.

A rare skin condition with dark, thick, warty patches and some hair loss was found in a newborn boy.

A woman with multiple autoimmune diseases showed improvement in hair loss but not in skin discoloration after treatment.

A boy had a rare scalp condition with thickened skin and different-colored hair.

A woman's hyperandrogenism was caused by a genetic mutation leading to non-classic adrenogenital syndrome.

The patient's hair has unique structural differences with alternating bright and dark bands.

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

The boy's symptoms suggest a possible new medical condition.

A cat's poor wound healing was linked to a genetic deletion in the COL5A1 gene.

A woman's liver was damaged by taking the herbal supplement Shou-Wu-Pian, but it got better after she stopped using it.

A black-skinned woman was diagnosed with Vogt-Koyanagi-Harada disease and treated with steroids and eye drops.

Early detection and multidisciplinary treatment are crucial for managing Papillon-Lefévre syndrome.

A 15-year-old girl with missed periods was diagnosed with a pituitary disorder and treated with hormones and steroids.

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

A man with a birthmark on his scalp developed hair loss that improved with treatment, but the link between the birthmark and hair loss was unclear.

Clouston syndrome causes issues with teeth, hair, nails, and skin, and has no cure, but recognition has improved.

Sebaceous gland atrophy and abnormal function may contribute to hair loss in psoriasis.

Early diagnosis and treatment of endocrine disorders like HAIR-AN syndrome can improve outcomes in adolescents.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

Biotinidase deficiency can mimic other conditions, making early diagnosis and treatment crucial to prevent lasting issues.

A 15-year-old girl has a skin condition causing blisters on her feet, likely inherited from her family.

Frontal Fibrosing Alopecia may be linked to autoimmune diseases like Sjögren's syndrome.

The girl's swelling and skin issues improved with fluid restriction and diuretics.

Macrophage activation syndrome can be a deadly first sign of systemic lupus erythematosus.

Doctors often diagnose Cushing's syndrome late, which worsens symptoms; earlier detection is needed.

Pilonidal sinus disease is linked to more severe hidradenitis suppurativa.

A 5-year-old girl with a rare genetic disorder, lipoid proteinosis, showed reduced new lesions but persistent scars after avoiding skin trauma.

Certain SPINK5 gene mutations are common in Israeli families with Comèl-Netherton syndrome.

Hair shaft changes may be linked to CCCA, but their role is unclear.