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A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

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

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

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

Accurate diagnosis of APL is crucial to avoid unnecessary treatments.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

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

The document concludes that various childhood hair and nail disorders exist, some may improve on their own, and advances in genetics and immunology could enhance treatment and counseling.

The WNT signaling pathway is important in many diseases and targeting it could offer new treatments.

The document concludes that understanding the genes and pathways involved in hair growth is crucial for developing treatments for hair diseases.

The article explains the genetic causes and symptoms of various hair disorders and highlights the need for more research to find treatments.

Effective management of children's hair loss involves accurate diagnosis, various treatments, and supportive care.

Some hair loss disorders are caused by genetic mutations affecting hair growth.

Accurate clinical, histological, and genetic methods are key for understanding and treating hair disorders.

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.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

Genetic discoveries are key for understanding, diagnosing, and treating inherited hair and nail disorders.

The document concludes that over 500 genes are linked to hair disorders and this knowledge is important for creating new treatments.

Researchers found a gene mutation responsible for a rare hair loss condition.

The document emphasizes the importance of correctly identifying and classifying genetic hair disorders to help diagnose related health conditions.

Changes in the HR gene have influenced hair growth and may lead to hair loss conditions in humans.

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

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

The unique coat of lykoi cats is likely caused by new variants in the Hairless gene.

Photodynamic therapy may not work for erythroplasia of Queyrat and could lead to invasive squamous cell carcinoma.

Genetic mutations cause various hair diseases, and whole genome sequencing may reveal more about these conditions.

The baby’s hair loss was due to a rare genetic condition, not treatable by usual methods.