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A patient with steroid sulfatase deficiency had a unique hair pattern and a brain malformation not previously linked to the condition.

A baby boy with 13q deletion syndrome had eye cancer, a woman's vision improved after stopping a breast cancer drug, a man developed cataracts from using Propecia, and a rare skin disorder called Lipoid Proteinosis was discussed. Also, a tool called OCT is useful for diagnosing macular diseases.

A patient had both chronic cutaneous lupus erythematosus and frontal fibrosing alopecia.

A scalp infection by Mycobacterium abscessus can cause hair loss even in healthy individuals and may be misdiagnosed.

A woman's sudden hair loss three years after a bone marrow transplant was a sign of chronic graft-versus-host disease but improved with treatment.

A rare benign tumor was found in a man's scrotum, highlighting the need for accurate diagnosis.

A thorough skin history and full examination are important for diagnosing and understanding the impact of skin diseases.

Atypical symptoms in lupus can indicate different kidney issues.

Atypical male hair loss may not respond to usual treatments.

A new syndrome, Teelwani Syndrome, combines features of two rare genetic disorders.

A girl with skin rashes and low zinc levels improved with zinc supplements and had new gene mutations linked to her condition.

A calf in Scotland likely had Schmallenberg virus from its mother.

A thorough skin history and examination are essential for diagnosing and treating skin conditions effectively.

A mother's PPARγ is crucial for preventing harmful milk that can cause inflammation and growth problems in babies.

A wearable device using electric stimulation can significantly improve hair growth.

A new protein was made to detect specific skin cell growth receptors and worked in normal skin but not in skin cancer cells.

A mutation in the KRT25 gene causes a rare hair disorder with thin, woolly hair.

A boy with severe Vitamin D-resistant rickets did not respond to treatment and lacked a common symptom, suggesting a need for alternative treatments.

A 3-month stay in space causes skin thinning, disrupts hair growth, and changes muscle-related genes in mice.

A specific enzyme is crucial for the bean plant's relationship with certain beneficial soil bacteria and fungi.

A PKP1 gene mutation causes skin fragility and hair loss in Chesapeake Bay retriever puppies.

A fungus is essential for forming and shaping hair ice on dead wood.

A 6-year-old girl was diagnosed with a rare hair disorder and started treatment with topical minoxidil.

A young woman with a rare hair loss condition improved with steroid and biotin treatment.

A 3-year-old boy had a rare hairball condition usually seen in teenage girls.

A 66-year-old man with a rare case of male frontal fibrosing alopecia did not regrow hair despite treatment.

A 2-year-old boy with a rare brain malformation may have Gomez–López-Hernández syndrome.

A rare genetic mutation found in an Indian family can be detected through prenatal screening.

A new method was created to measure metformin in hair, showing potential for monitoring treatment and medical investigations.

A low-power, fast laser safely reduces hair with minimal pain and few side effects.