Search

everythingexperts & clinicslearnresearchcommunity

for

Search:↓

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.

People with Alopecia Areata have more herpes simplex infections but similar rates of cancer, blood clots, and heart disease compared to those without it.

The human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.

Antiandrogen therapy may help treat hidradenitis suppurativa.

Antiandrogen therapy may be beneficial for women with hidradenitis suppurativa.

A woman with Sheehan syndrome improved with hormone treatment.

Older parental age, rural living, and specific genetic mutations increase hypospadias risk in children.

Potential androgen excess signs vary by demographics and health, needing inclusive evaluation.

This rare genetic disorder causes permanent hair loss and skin bumps from birth.

Acne is common and can be linked to various systemic health conditions and syndromes.

About 13% of women had idiopathic hirsutism and 8.5% had polycystic ovary syndrome in a group of Iranian women.

A mutation in the HOXC13 gene causes hair and nail problems in a Syrian family.

Certain gene variations might be linked to severe acne in women but not in men.

AGA can occur in children with family history; early diagnosis and treatment important.

Men with early hair loss may have higher health risks similar to women with PCOS.

Certain HLA class II alleles increase or decrease the risk of alopecia areata.

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

Early-onset hair loss in Egyptian males is linked to genetics, hormones, and lifestyle factors like smoking and diet.

There's no clear link between female pattern hair loss, insulin resistance, and metabolic syndrome.

A new genetic mutation was found causing hair and eye issues in a boy.

The patient has a rare skin condition that shows features of two known disorders.

Hormonal imbalances in congenital adrenal hyperplasia cause acne.

Netherton syndrome in a boy caused skin and hair issues, and treatment didn't work.

A rare genetic mutation caused severe symptoms in a 6-year-old girl with mandibuloacral dysplasia type A.

The MBTPS2 gene variant c.970+5G>A is a common mutation causing IFAP syndrome.

Dermatologists should consider congenital syndromes like TRPS in young adults with early hair loss.

Alopecia areata in Taiwan has a high disease burden and needs better research and diagnostic criteria.

A girl with hereditary chorea, likely Huntington's disease, had her condition worsened by lupus.

Alopecia areata patients are more likely to have thyroid disorders than healthy individuals.

Managing rare genetic diseases like osteogenesis imperfecta and Escobar syndrome is complex and requires both medical and surgical treatments.