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The G60S Connexin43 mutation causes hair growth issues and poor hair quality in mice, similar to human ODDD patients.

A man with Acrodermatitis continua did not get better with etanercept treatment, and his condition worsened, suggesting treatment effectiveness may vary by genetics and race.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

Benzoyl peroxide and adapalene gels work differently to reduce acne in mice.

Dermatoscopy is a useful tool for diagnosing hair disorders and can help choose samples for more detailed analysis.

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

Patients with Bohring-Opitz syndrome and ASXL1 mutations need regular kidney ultrasounds to check for tumors.

Impaired androgen production in 46,XY DSDs causes ambiguous genitalia and requires long-term care.

Trichoscopy is a useful tool for diagnosing hair disorders without pulling out hair.

Most hair loss in children is caused by a few common conditions, and it's important to diagnose these properly and support the child's mental health.

The document concludes that eyelash trichomegaly, which is the abnormal growth of eyelashes, can be present from birth, caused by diseases, or result from certain medications.

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 document concludes that periocular hair disorders have various causes and treatments, and proper evaluation by specialists is important for management and prognosis.

The document concludes that various hair and scalp disorders in children have specific treatments and proper diagnosis is essential.

Early treatment of acne is crucial to prevent scarring and psychological effects.

The guide helps doctors diagnose hair problems by suggesting a thorough patient history, physical exams, and various diagnostic tools.

The document concludes that proper diagnosis and treatment of hair shaft disorders require understanding their unique causes and avoiding hair-damaging practices.

Understanding normal hair growth and loss in children is key to diagnosing and treating hair disorders.

Genetic mutations can affect female sexual development, requiring personalized medical care.

A new TP63 mutation was found in a baby with EEC syndrome, showing the need for TREC testing to check for immune issues.

Genetic factors play a major role in acne.

Increased FGFR2b signaling, influenced by androgens, plays a role in causing acne.

A 6-year-old girl was diagnosed with a rare hair disorder and started treatment with topical minoxidil.

Rapp-Hodgkin syndrome, AEC, and EEC are different expressions of the same genetic disorder caused by TP63 gene mutations.

Pili torti is a rare condition where hair is twisted and breaks easily, often linked to genetic disorders or other health issues.

A special clotrimazole varnish cured a siamang's persistent skin infection after 3 months.

Bardet-Biedl syndrome may include under-recognized skin problems related to its metabolic disturbances.

Gibbons at Tegal Alur Animal Rescue Center need better feed management to improve their health and weight.

Ketoconazole cream is effective for skin conditions like seborrheic dermatitis and may help with hair loss and other skin issues, with generally mild side effects.

Diagnosing sex development disorders requires combining medical history, physical exams, imaging, lab tests, and genetic data.