Search

everythinglearnresearchcommunity

for

Search:↓

A woman with Budd-Chiari syndrome improved after treatment and needs a liver transplant, highlighting the importance of considering non-criteria antiphospholipid syndrome in similar cases.

Pili torti hair twists due to uneven outer root sheath cell development.

A new genetic mutation in the hairless gene causes a rare hair loss disorder.

Two boys had a rare skin condition needing to be differentiated from similar disorders, with unclear inheritance due to few cases.

The document concludes that syphilis has varied symptoms that are often missed, making clinical awareness crucial for diagnosis.

Dilated pupils can be an early sign of HIV/AIDS.

A family showed a new condition with inherited hair loss and skin changes, possibly due to one genetic disorder.

A 23-year-old Syrian woman has two rare hair disorders, and avoiding hair treatments plus using vitamins and minoxidil may help.

Hutchinson-Gilford Progeria Syndrome causes rapid aging from a genetic mutation, with no cure but ongoing research into potential treatments.

Systemic Lupus Erythematosus has varied symptoms and is hard to diagnose, affecting many body parts and requiring careful clinical judgment.

Middle-aged women in Iran are most affected by primary cicatricial alopecia, especially discoid lupus erythematous.

Björnstad syndrome can cause hair loss similar to androgenetic alopecia, and treatment with baricitinib and minoxidil may help.

A rare skin condition usually on the face was found on a man's heel.

Women with nonclassical congenital adrenal hyperplasia may have a higher risk of fertility issues and miscarriages, and should get genetic counseling.

A child with eruptive vellus hair cysts showed some improvement with calcipotriene cream.

Cystic panfolliculoma is a rare, harmless tumor that can be confused with other skin tumors.

A woman had a rare liver tumor causing male-like physical changes, highlighting the need for thorough checks when such symptoms appear.

Pseudo-Cushing's symptoms disappear once the underlying issue is resolved.

The girl's unexpected pubic hair growth led to a diagnosis different from complete androgen insensitivity syndrome.

Elderly patients with CCCA were all African American with low vitamin D, but no iron or zinc deficiencies, and no hormonal imbalances compared to younger patients.

Type B Insulin Resistance Syndrome is rare, linked to lupus, and hard to treat due to severe insulin resistance.

A woman was diagnosed with Sheehan's syndrome and a rare complication of diabetes insipidus 33 years after symptoms began, improving with hormone therapy.

Giant keratoacanthoma can look like squamous cell carcinoma, requiring careful diagnosis and surgical removal.

The patient showed signs of liver disease due to alcohol use but didn't need treatment for Dupuytren’s contracture.

Carcinosin, a homeopathic remedy, helped a young girl with alopecia areata regrow hair and reduce psychological symptoms.

A rare genetic mutation causes severe immune issues, hair loss, and nail problems.

A woman developed white patches on her skin and curly hair after hepatitis C treatment, likely due to the medication interferon alpha.

A man with a rare lung-focused form of hypereosinophilic syndrome improved with steroid treatment.

The document reports the 19th global case of a rare skin condition in a patient from Colombia.

A 16-year-old girl's skin rash was likely caused by an infection and improved with topical steroids.