Search

everythinglearnresearchcommunity

for

Search:↓

The study concluded that a protein important for hair strength is regulated by certain molecular processes and is affected by growth phases.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

Hair loss in androgenetic alopecia is caused by genetic factors and androgen excess, and can be treated with combined therapies.

A baby girl has a hair disorder called monilethrix, causing fragile hair that may improve over time.

Dermatopathia pigmentosa reticularis causes skin discoloration, hair loss, and nail problems.

A family showed a new condition with inherited hair loss and skin changes, possibly due to one genetic disorder.

Trichoscopy helped diagnose a teenage girl's hair loss as monilethrix.

KFSD is a genetic disorder causing hair loss and skin issues, with no effective treatment.

An 18-year-old man was diagnosed with a rare genetic disorder causing hair loss, severe light sensitivity, and skin issues.

A 12-year-old boy with a rare genetic condition has progressive hair loss with no effective treatment.

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.

Monilethrix causes fragile, patchy hair loss.

Most patients with hair loss sought treatment for cosmetic reasons, were unhappy about their appearance, and had a family history of the condition, suggesting it may be inherited.

Monilethrix causes different levels of hair loss in family members.

CCCA is a common hair loss condition in African American women, often inherited and influenced by hairstyling, with unique scalp features detectable by special tools.

A 12-year-old girl was diagnosed with monilethrix, a genetic condition causing fragile, beaded hair that breaks easily, with no effective treatment available.

A woman's hair changed to a dry, tangled texture that's hard to comb after treatment with spironolactone, suggesting the medication might cause such hair changes.

The document concludes that the girl's hairlessness is likely inherited from her parents.

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.

A new genetic disorder caused by an ODC1 mutation can be treated with DFMO.

An 11-year-old girl with a rare skin disorder also had cornea issues and dry eye, needing careful management.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

Loose Anagen Hair Syndrome is a hereditary condition causing hair loss in children due to abnormal hair follicles.

Monilethrix is a genetic hair disorder causing fragile, beaded hair with no effective treatment.

Mother and son diagnosed with a rare genetic hair loss condition with no effective treatment.

A boy and his father with hereditary hypotrichosis simplex were treated for hair loss, but the treatment result is unknown.

Genetic testing is crucial for diagnosing congenital atrichia, a rare condition causing irreversible hair loss.

A person with a specific gene mutation had extra teeth, unique jaw and hair features not seen before in this condition.

The document explains how to identify different hair problems using a microscope.

A 2-year-old girl had a hair disorder not shared by her identical twin.