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A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

Giving a special protein to dogs with a certain genetic disease improved their symptoms but didn't help with hair growth.

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

New gene mutations linked to skin conditions were found, bacteria and chemicals may worsen acne, a dog mutation could exist in humans, virus-like elements might be involved in psoriasis, and a vitamin D3 treatment doesn't prevent chemotherapy-related hair loss.

Scientists now better understand the genetics of hypohidrotic ectodermal dysplasia, leading to more accurate diagnoses and potential new treatments.

The gene for Clouston syndrome in a large Indian family is located in the 13q11-q12.1 region.

Lactic acid cream can help improve skin bumps known as eruptive vellus hair cysts.

Hair loss in Cronkhite-Canada syndrome may be caused by autoimmune factors, not just stress or malabsorption.

Kampo medicine can help treat general fatigue from long COVID.

Low-level laser therapy may help regrow hair in dogs with non-inflammatory hair loss.

An 8-year-old Saudi boy was diagnosed with a rare genetic disorder causing hair loss, skin issues, and light sensitivity.

The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

Hair, teeth, and mammary glands develop similarly at first but use different genes later.

Permanent hair removal with lasers may cure itchy black hair bristles on the back.

Sonidegib and vismodegib are similarly effective for advanced basal cell carcinoma, but sonidegib might have a slightly better safety profile.

Rituximab may be an effective treatment for Cronkhite-Canada syndrome with kidney disease.

Children's hair loss can be caused by various factors and should be treated with appropriate, age-specific methods and psychological support.

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

Clouston syndrome is inherited in an autosomal dominant pattern and caused by a specific gene mutation, with no current treatment available.

Cronkhite-Canada syndrome can be diagnosed without gastrointestinal polyps if there is severe mucosal atrophy and edema.

Human hair keratins K85 and K35 create unique filament patterns important for early hair formation.

Trichoscopy is a quick and easy way to diagnose most genetic hair problems without invasive methods.

Different genes are linked to various types of hair loss.

Monilethrix causes different levels of hair loss in family members.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

Patients with Shwachman-Diamond syndrome often get misdiagnosed due to a wide range of symptoms, including immune system problems and bone abnormalities.

Early recognition and treatment of VATS in transplant patients improve outcomes.

Hormone imbalances can cause specific skin changes, which may help in early detection of endocrine disorders.

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

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