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Personalized thiopurine dosing based on NUDT15 genotyping can improve long-term outcomes for ulcerative colitis and Crohn's disease patients.

A child has a rare hair and skin disorder due to specific gene variants, suggesting broader genetic testing is needed.

Dr. Russell Knudsen's system classifies hair grafts by class, shape, and size for clearer communication in hair restoration surgery.

Trichoscopy is a useful tool for diagnosing different hair and scalp diseases without surgery.

The conclusion is that the variation in hair thinness in patients is mostly due to the amount of underdeveloped hairs, and treatments that thicken fine hairs might work for those with mild to severe conditions.

Deep phenotyping helps distinguish between xeroderma pigmentosum and trichothiodystrophy, aiding in diagnosis and treatment.

A woman's hair loss looked like a different condition due to her hairstyle, and treatment stopped further hair loss but didn't regrow hair.

Topical minoxidil can help improve hair in trichonodosis.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

A new genetic mutation in the CDH3 gene causes hair loss and eye problems in young people.

Trichostasis spinulosa is a common but often unnoticed skin condition involving bundled vellus hairs, especially in people with darker skin or UV exposure.

Trichilemmal cysts may form from hair follicle outer root sheath growth.

Two babies needed surgery to remove hair tightly wrapped around their toes to prevent serious injury.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

A rare hair follicle tumor was found on a woman's vulva.

Educating healthcare workers and parents about hair toe tourniquets can help prevent serious complications.

Trichoscopy is a tool for detailed examination of hair and scalp diseases.

Trichostasis spinulosa is a rare skin condition with hair-filled plugs in hair follicles.

The specific skin disease variant p.(Arg2000Trp) in plectin can cause a wide range of symptoms, which should be considered when diagnosing patients.

The length of the CAG repeat in the androgen receptor gene affects the risk and progression of prostate cancer, BPH, infertility, and undermasculinized genitalia.

A preterm baby's toes were saved from damage by quickly removing a thread that was cutting off circulation.

Hair-thread tourniquet syndrome needs more awareness and discussion in dermatology.

A young athlete's fragile hair condition improved by cutting hair and using gentle shampoo.

Mutations in the TSPEAR gene cause a new form of ectodermal dysplasia affecting hair and tooth development.

A 16-year-old girl with a hair-eating disorder needed surgery to remove a hairball from her stomach and small bowel.

A new therapy for a skin blistering condition has not been developed yet.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

A child died from eating hair, causing severe stomach blockages and infection.