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Ectodysplasin signaling is crucial for skin appendage development, requiring specific doses and durations.

Tissue-specific variation in mutant load complicates genetic counseling and prenatal diagnosis.

A baby girl had two brain-related growths removed and is developing normally.

Recent progress has been made in understanding inherited hair and nail disorders.

Oxytocin receptor changes in hair cells may help identify autism, especially in males.

Growth factors greatly affect hair loss, with different levels seen in men, women, younger patients, and at the start of the condition.

Poor maternal nutrition can lead to fewer wool follicles in Chinese Merino sheep.

The girl with autoimmune hair loss might regrow hair within a year, and treatments can help but not prevent recurrence; dermatologist referral and corticosteroids are recommended.

Human alpha defensin 5 helps heal wounds, reduce bacteria, and grow hair on burned skin.

Blocking the mineralocorticoid receptor can help treat skin thinning caused by steroids.

Molecular diagnostics help identify genetic defects causing endocrine diseases, improving diagnosis and treatment options.

The commentary stresses the importance of using historical control data and proper interpretation in evaluating developmental toxicity.

Kallmann syndrome can cause eye issues and other health problems, requiring various treatments.

Taking vitamin B6 corrected a pregnant woman's metabolic disorder, which changed her hair color.

Understanding skin structure and development helps diagnose and treat skin disorders.

Epidermolysis bullosa simplex causes easily blistered skin due to faulty skin cell proteins, leading to new treatment ideas.

The document explains how to create detailed biological pathways using genomic data and tools, with examples of hair and breast development.

Mothers with alopecia areata have a higher risk of adverse birth outcomes.

Pregnant women with COVID-19 and gestational diabetes may face severe complications, and more research is needed on their outcomes.

Hair follicle development and microbes help regulatory T cells gather in newborn skin.

PRP helps skin heal, possibly through special cells called telocytes.

S100A3 protein is crucial for hair shaft formation in mice.

Early diagnosis of Trichorhinophalangeal syndrome type 1 is crucial for treatment and was achieved through clinical examination and family history.

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

Adults should not consume more than 255 micrograms of selenium per day to avoid risk of hair loss and other side effects.

Fish oil improves skin health in people with diabetes and high cholesterol.

A genetic change in the EDAR gene causes the unique hair traits found in East Asians.

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

Pregnant women with Systemic Lupus Erythematosus have a higher risk of blood clotting problems.

Zinc is crucial for growth and health in rats.