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A patient with Ivemark syndrome developed mixed type vitiligo after a hepatitis C infection, showing different treatment responses and immune cell involvement in the skin.

Isotretinoin reduced inflammation in tufted hair folliculitis, but hair tufting remained.

The hr gene is crucial for skin and hair health, with mutations causing hair disorders.

Patients often experience long-lasting changes to their hair after stem cell transplants.

Parental support and gender-affirming care are crucial for the mental health of transgender adolescents.

A new classification for trichothiodystrophy helps identify genetic causes and potential treatments.

Surgical excision is the best treatment for SCC, but intralesional cidofovir might be a good alternative.

The hamster polyomavirus middle T antigen is linked to tumors in hamsters and associates with a specific tyrosine kinase.

The study found two new mutations in a Chinese patient with severe biotinidase deficiency.

A new method effectively measures nicotine and cotinine in blood and urine for forensic analysis.

Men with CCCA often face delayed diagnosis and severe hair loss, highlighting the need for earlier recognition and treatment.

A 25-year-old man with multiple skin tumors was successfully treated with acitretin and methotrexate.

Trastuzumab may cause tufted hair folliculitis as a side effect.

Traditional Chinese medicine may help relieve symptoms of Cronkhite-Canada syndrome.

A specific gene mutation causes different hair defects in Indian monilethrix families.

A baby boy's toe was saved from damage caused by hair strangulation by quick surgical treatment.

Loss of TET2 increases the risk of skin and oral cancer.

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

Different human hair keratin types have unique structures that affect how they dissolve and can be used to create self-tendons.

Tgm2 helps stabilize dying cells and aids fibroblast attachment to the extracellular matrix.

The trichohyalin gene is located at chromosomal region 1q21 with other skin-related protein genes.

CXXC5 is a protein that prevents hair growth and could be a target for hair loss treatment.

Tunisian children with hereditary vitamin D-resistant rickets showed improvement with calcium treatment, and new genetic mutations were identified.

Finasteride and CPA-EE2 equally reduce hirsutism, but affect hormone levels differently.

There is no standard treatment for the rare Cronkhite–Canada syndrome, which can be fatal and lead to cancer.

Most patients experienced hirsutism again after stopping hormone treatment, indicating long-term treatment is needed to maintain results.

Higher homocysteine levels may inhibit hair growth and are linked to androgenetic alopecia.