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Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

Doctors should consider Netherton syndrome in patients with chronic skin and hair issues to avoid misdiagnosis.

Mice with extra human KLK14 had hair and skin problems, including weaker cell bonds and inflammation, linked to Netherton syndrome.

The document says that treating the root cause of hair follicle damage is crucial to prevent permanent hair loss, and treatment options vary.

Researchers found a new genetic mutation causing a rare hair loss condition in the first Japanese child studied.

Adjusting the medication tacrolimus resolved a boy's red nail beds after a stem cell transplant.

The conclusion is that an algorithm using trichoscopy helps diagnose different types of hair loss but may need updates and a biopsy if results are unclear.

A new mutation in the HR gene causes hair loss in a specific family.

The most common cause of hair loss in children is tinea capitis, followed by alopecia areata and telogen effluvium.

The document concludes that an experimental drug may help wound healing in Epidermolysis Bullosa, links Hydroa vacciniforme to EBV, discusses diagnosing hair loss disorders, finds many children with eczema have allergies, reviews the safety of a skin medication in children, notes side effects of a Duchenne's treatment, and identifies a marker for pediatric mastocytosis.

New markers and pathways have been found in skin tumors, helping better understand and diagnose them.

Steatocystoma multiplex causes recurring skin cysts and needs early recognition for better management.

A baby had a rare case of widespread milia, which was treated and is being monitored.

Children's hair grows in different types from before birth through puberty, with growth rates and characteristics varying by age, sex, and race.

A woman's hair turned gray and fell out after starting a cancer drug called imatinib mesylate.

Neurohormones help control skin health and could treat skin disorders.

The document concludes that managing skin conditions during pregnancy is important and requires specialized care.

FGF13 gene changes cause excessive hair growth in a rare condition.

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

Cantú syndrome is caused by mutations in the ABCC9 gene.

Cantu syndrome, which causes excessive hair growth and skin issues, is due to a mutation in the ABCC9 gene, and understanding this could help develop new treatments for hair diseases.

Two specific SNPs in the TRPS1 gene cause excessive hair growth by altering the protein's structure.

Hypertrichosis lanuginosa causes excessive fine hair growth, often linked to genetics or cancer, with limited treatment options.

Different hair and scalp disorders cause hair loss or excess hair growth, with various treatments available depending on the specific condition.

The document reviews various hair and nail disorders, their causes, and treatments, emphasizing the need for proper diagnosis and the link between nail changes and systemic diseases.

Monilethrix is a rare, inherited condition causing fragile hair and hair loss, with no cure but some treatments may help.

Finasteride caused blisters on hands and feet.

K_ATP channel gene mutations are linked to heart diseases, but more research is needed to understand the connection and treatment potential.

The document concludes that accurate diagnosis and appropriate management are crucial for treating various hair disorders, which have significant psychological impacts.