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Most women with hirsutism or androgenic alopecia had polycystic ovaries, especially if they had irregular periods.

A genetic mutation in the CDH3 gene causes hair loss and vision problems in a young Saudi girl.

The treatment improved acne, seborrhoea, and hirsutism, with some side effects like spotting and nervousness.

The review concluded that restrictions on people with HIV/AIDS often violated their rights without proven effectiveness in stopping the virus, highlighting education as the best control method.

Surgery is the main treatment for liver hydatidosis, but has risks; albendazole is the most effective drug but can have side effects.

Three siblings with a genetic form of rickets showed different symptoms of the disease.

The case suggests a possible autoimmune link between lichen sclerosus and vitiligo.

Acyclovir can prevent rejection of skin grafts in herpes-related lip leucoderma.

RHUPUS should be considered in children with deforming arthritis.

Early recognition and aggressive treatment can significantly improve rare ANA-negative lupus with heart and skin issues.

The HSD3B1 variant increases hair loss risk in overweight women with PCOS.

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

A man with KID syndrome developed a rare cancer in a long-term skin infection.

Skin ulcers from interferon may not depend on the amount given.

Most kidney transplant patients in the study had skin problems, often related to infections, medication side effects, or skin cancer risks.

Men, diabetes, and high inflammation levels lead to higher COVID-19 antibodies.

Two siblings with a genetic mutation had a form of rickets that doesn't respond to vitamin D.

Rapid virilization should be checked for possible ovarian or adrenal cancer.

About 2.2% of women with symptoms of high male hormones have a mild form of congenital adrenal hyperplasia, and measuring a specific hormone level can accurately diagnose it.

Young patients with Vogt-Koyanagi-Harada syndrome may have poor vision outcomes despite treatment due to frequent recurrences.

Sertoliform endometrioid carcinoma of the ovary, though rare, has a good prognosis when treated early.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

SHBG binding properties are unchanged in male liver cirrhosis patients.

Autoimmune reactions may cause both alopecia areata and HAM.

A 16-year-old boy with Castleman's disease and lupus was successfully treated and showed no recurrence.

A rare, non-cancerous ovarian tumor was successfully treated with surgery, improving the patient's symptoms.

An 87-year-old man showed unusual signs of Hodgkin lymphoma, primarily high calcium levels, which improved after treatment and revealed the disease.

Young HS patients often have other physical and mental health issues, and research on HS covers a wide range of topics including genetics, triggers, treatments, and the need for more data.

Testing basal 17-HP levels is a good way to screen for nonclassic adrenal hyperplasia in women with high androgen levels.

Kaposi's sarcoma lesions might originate from benign tissue changes.