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The gene Prss53 affects hair shape and bone development in rabbits.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

A girl with Becker's nevus syndrome showed good improvement in breast development using spironolactone.

A Brazilian male with IFAP syndrome has a unique genetic variant causing his condition.

Isotretinoin can cause serious birth defects and needs careful use, especially in pregnant women.

CAH is a genetic disorder affecting cortisol production and causing hormonal imbalances, with treatment and diagnosis varying by form and symptoms.

NEMO syndrome and systemic lupus erythematosus are linked in a new disease association.

Fibroblast growth factor receptor signaling controls cell development and repair, and its malfunction can cause disorders and cancer, but it also offers potential for targeted therapies.

The document concludes that early diagnosis and treatment of Congenital Adrenal Hyperplasia are crucial for preventing serious health issues and improving patient outcomes.

New genes and pathways are important for testosterone production and male sexual development.

Minoxidil is mostly safe, but high doses can cause electrolyte imbalances and heart issues in dogs.

Ancient Chinese goats evolved cashmere-producing traits due to selective breeding, particularly in genes affecting hair growth.

R-spondins and their receptors help increase bone growth and may be used to treat bone loss diseases.

Acitretin is effective for severe psoriasis and can be used long-term due to no immunosuppression, but must be carefully monitored for side effects and is not for pregnant women.

Genetic defects in testosterone production can cause hormonal and developmental disorders, and more research is needed to understand androgen regulation and develop safer treatments.

LAAM caused developmental toxicity in tolerant rats without causing birth defects.

Antiandrogens can treat female hormonal conditions, but environmental ones may harm reproductive health.

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

Gene mutations can cause problems in male genital development.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Topical tofacitinib is effective and safe for treating alopecia areata.

A 19-year-old male with delayed puberty was successfully treated for a condition that prevents normal hormone production.

A patient with Rothmund-Thomson syndrome showed skin changes, hair loss, and dental defects but no cataracts or skeletal issues.

A new medical syndrome may include skin changes, hair loss, sweating issues, bone malformations, leg swelling, and low cortisol.

Oral retinoids can cause side effects ranging from mild to severe, including birth defects, and require careful monitoring and contraception.

Systemic retinoids are effective for psoriasis but have side effects; benefits may outweigh risks, especially when reducing cancer risks from other treatments.

Treat adult facial vascular anomalies with lasers, surgery, or observation, depending on the patient's specific condition.

Metformin helps regulate menstrual cycles, induce ovulation, and improve pregnancy outcomes in women with PCOS.

Wnt7a protein is crucial for development and tissue maintenance and plays varying roles in diseases and potential treatments.

Treat pediatric skin issues with accurate diagnosis, multidisciplinary team, and various treatment options.