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Mutations in the PTPRQ gene cause significant balance issues in mice due to hair bundle defects in the inner ear.

Hidradenitis Suppurativa is a chronic skin condition best treated early with surgery for better outcomes and less recurrence.

Inherited ichthyoses cause widespread skin scaling and thickening due to gene mutations.

Over 67 genes linked to ichthyosis help improve diagnosis and treatment.

Understanding the genetics of rare inherited ichthyosis syndromes is key for better treatments and genetic counseling.

BMP4-related anomalies can cause a wide range of eye, brain, and hand/foot problems, and new cases show this variability.

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

Skin healing from blisters can delay hair growth as stem cells focus on repairing skin over developing hair.

Ayurveda's descriptions of genetic disorders align with modern genetic understanding.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

An 11-year-old child with total hair loss may have a genetic autoimmune disease, and the outlook for hair regrowth is not good.

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

A KRT71 mutation in Hereford cattle in Uruguay causes thin, curly hair and scaly skin.

Wnt signaling is important for development and cell regulation but can cause diseases like cancer when not working properly.

Increased HIF-1α is linked to the inflammation and severity of hidradenitis suppurativa, suggesting treatments that lower HIF-1α could help.

Early diagnosis and tailored treatments are crucial for managing ichthyosis syndromes with hair abnormalities.

Acne is linked to inflammation and insulin resistance, and is associated with various syndromes that require different treatments.

Hidradenitis Suppurativa is likely an autoinflammatory disease, and better understanding its causes could improve treatments.

Acanthosis nigricans is a skin condition that may indicate a higher risk for insulin resistance and type 2 diabetes, and more research is needed to understand and treat it.

Acne is significantly influenced by genetics, and understanding its genetic basis could lead to better, targeted treatments.

Researchers created a mouse model for Cushing's syndrome to study glucocorticoid excess and potential treatments.

When skin blisters, healing the wound is more important than growing hair, and certain stem cells mainly fix the blisters without helping hair growth.

The cornified envelope is crucial for skin's barrier function and involves key proteins and genetic factors.

Children's screen time increased during the pandemic, causing various health issues.

Hidradenitis suppurativa is a chronic skin condition more common in women, linked to genetics and lifestyle factors, and associated with various other health issues.

The book details advanced techniques in cosmetic dermatology for experienced surgeons.

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

Nursing staff's mental health was affected during the COVID-19 pandemic.

FFA's causes may include environmental triggers and genetic factors.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.