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A new severe form of monilethrix syndrome includes hair loss, scalp itching, cataracts, and distinct facial features.

Early diagnosis and genetic evaluation of ADULT syndrome are crucial to reduce stress and medical costs.

A woman with a new PTCH gene mutation has both Gorlin syndrome and severe hair loss.

Old people's nails often have problems due to body changes, more diseases, and self-care difficulties, affecting their movement and hand use.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

A family was found with both Trichorhinophalangeal syndrome and Loose Anagen Syndrome, suggesting a genetic connection.

A man's crushed thumb caused unusual horizontal nail ridges on all fingers of one hand.

A 19-month-old boy with a rare hair disorder showed mild improvement with treatment, but his family chose gentle hair care due to limited success.

Porokeratotic eccrine and hair follicle nevus is a very rare skin disorder possibly caused by a GJB2 gene mutation.

A 17-year-old girl and her brothers have a rare hair condition with long eyelashes, thick eyebrows, and easily pluckable hair.

Two siblings both had a rare case of alopecia areata at the same time.

Hair casts, also called pseudonits, are often mistaken for other conditions.

A 6-year-old girl was diagnosed with a rare hair disorder called monilethrix.

Thymoma may link myasthenia gravis, nail dystrophy, and alopecia areata.

Two siblings had a rare hair condition with banded hair, which doesn't need treatment.

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

A rare gene variant causes hair and nail issues in a family.

A 12-year-old girl's hair loss was linked to a rare genetic condition called ALX4-related frontonasal dysplasia.

The man was diagnosed with Cronkhite-Canada syndrome, a rare disorder with GI polyps, skin issues, hair loss, and nail problems.

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

Zinc treatment improved skin and hair issues in a boy with a zinc-related condition.

A child with skin and tooth symptoms was found to have a genetic mutation causing cardiocutaneous syndrome, leading to heart problems.

Papular acantholytic dyskeratosis of the vulva is a rare, benign skin condition that can be managed conservatively.

The study found no common cause for a girl's crystalline cataract and uncombable hair, suggesting their co-occurrence might be coincidental.

Mutations in the hairless gene cause hair loss and skin cysts in rhesus macaques.

A boy with Oculodentodigital syndrome had a unique GJA1 gene mutation causing his symptoms.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

Onychomatricoma is a unique nail tumor that mimics the entire nail unit and is not related to other hair-related tumors.

A 6-year-old girl had both monilethrix and trichorrhexis nodosa, causing brittle hair, with minimal improvement from treatment.