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A mother and daughter have a rare genetic hair loss disorder with no effective treatment.

Marie-Unna Hereditary Hypotrichosis is a rare genetic condition causing sparse hair growth, requiring specific recognition for proper care.

New hair transplant methods offer more natural results and better graft survival, with ongoing research to increase donor hair options.

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

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.

A Saudi girl was diagnosed with Loose Anagen Hair Syndrome, a rare condition causing easy hair loss without scarring.

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

Androgens can both stimulate and cause hair loss, and understanding their effects is key to treating hair disorders.

Loose anagen hair syndrome, often affecting young girls, can be diagnosed with a hair-pull test and usually gets better on its own, but severe cases may need treatment.

A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.

The document concludes that early diagnosis and treatment are crucial for children with hair loss to prevent permanent damage, although not all conditions can be effectively treated.

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

Some children who had stem cell transplants developed permanent hair loss, especially when treated with a drug called busulphan.

A 2-year-old boy had no hair and unusual organ placement, and it's unclear if it's genetic or coincidental.

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

A KRT71 mutation in Hereford cattle in Uruguay causes thin, curly hair and scaly skin.

An 8-year-old girl has a rare, irreversible hair loss condition caused by a genetic mutation.

A man with severe hair loss and skin disease regrew his hair with no side effects after taking tofacitinib.

A girl inherited excessive body hair from her mother and grandmother.

A rare genetic disease causes sparse hair and early blindness due to a gene mutation.

Hair transplant combining scalp and beard hair with PRP was successful for scarring alopecia.

No effective treatment exists to stimulate hair growth in atrichia with papular lesions.

The patient's long-term hair loss was caused by leukemia treatments and low estrogen levels, worsened by her genetic tendency for hair loss.

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.

Chemotherapy may cause recurring hair loss due to an autoimmune response.

The document concludes that understanding hair and feather regeneration can help develop new regenerative medicine strategies.

A cancer drug called nilotinib might cause hair loss due to inflammation around hair follicles.

Normal levels of DHT can reduce belly fat and increase muscle, but too much can lead to hair loss, prostate issues, and possibly heart disease.

Dermatologists are essential in helping transgender and gender diverse patients with skin and hair issues related to gender affirmation and hormone therapy.

Six genetic conditions are often linked to complete scalp hair loss in children.