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HTLV-1-associated lichenoid dermatitis (HALD) is linked to an immune response against HTLV-1-infected cells.

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.

Higher HDAC1 levels in alopecia areata suggest HDAC inhibitors might help treat it and acne.

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

New treatments offer hope for better managing hidradenitis suppurativa.

Hirsutism is abnormal male-pattern hair growth in females due to excess androgens.

Hidradenitis suppurativa is a complex, non-infectious skin condition with no single cause, difficult to treat, and greatly affects quality of life.

Hirsutism is excessive hair growth in women often caused by polycystic ovarian syndrome, and identifying the cause is important for managing associated health risks.

Facial hidradenitis suppurativa can be mistaken for acne but requires different treatment.

Balding men have harder scalps.

Hirsutism in teens is often due to polycystic ovarian syndrome and needs careful assessment and support.

Certain genetic markers, especially the MICA gene, are linked to alopecia areata.

The mutation causes hairless mice due to mislocalized and dysfunctional HR protein.

Hair antiretroviral concentration is affected by hair type, segment position, housing, drug use, sexual behavior, kidney function, and genetics.

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

Early recognition of skin lesions in Birt-Hogg-Dubé syndrome is crucial for detecting renal tumors early.

Children with classic congenital adrenal hyperplasia have thicker heart fat and are at higher risk for heart problems and early atherosclerosis.

All women with significant unwanted hair growth have hormonal imbalances, often from polycystic ovary syndrome.

Hirsutism perception varies by culture and individual.

Congenital atrichia with papular lesions is often misdiagnosed, and new diagnostic criteria can improve accuracy.

A misdiagnosed case of HAIR-AN syndrome led to unnecessary surgeries and highlighted the importance of correct diagnosis and treatment.

Most genetic mutations causing hypohidrotic ectodermal dysplasia in Russian patients are found in the EDA gene.

Hidradenitis suppurativa might be a type of autoinflammatory skin disease.

Coudability hairs are useful markers for alopecia areata activity.

THA is a rare condition with no significant clinical consequences if thyroid function is normal.

Uncombable hair syndrome causes frizzy hair and can affect the nervous system, eyes, and ears, often co-occurring with other hair, skin, nail, and teeth conditions, and is linked to three specific gene mutations.

Boys with less severe EDA mutations in XLHED have milder symptoms and better sweat and hair production.

A patient with HAIR-AN syndrome, PCOS, and Hashimoto's thyroiditis improved with early diagnosis and treatment to prevent serious health problems.

The RHD4 gene is crucial for consistent root hair growth in Arabidopsis thaliana.

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.