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Patients with mandible reconstruction had better quality of life and function than those with soft-tissue reconstruction.

Hair transplant complications were likely due to deep graft placement and rough handling.

Lampreys have a functional vitamin D receptor that may help detoxify harmful substances.

The STIM1 R304W mutation in mice leads to bone changes and teeth hair growth.

Congenital atrichia is a rare condition where children are born without hair, and treatment is often ineffective.

Pregnancy can cause skin changes and affect existing skin conditions, with limited treatment options due to the need for fetal safety.

Different ectodermal organs like hair and feathers regenerate differently, with specific stem cells and signals involved in their growth and response to the environment.

The TGF-β family helps control how cells change and move, affecting skin, hair, and organ development.

Pregnancy causes skin changes like darkening, hair thickening, nail changes, and increased risk of skin growths, most of which usually resolve after birth.

Hair loss improved with treatment and successful transplant.

Stem cell therapies show promise for hair regrowth in androgenetic alopecia.

Ptch2 plays a key role in controlling stem cell function and the ability to regenerate after birth.

Mutations in the Vitamin D receptor gene can cause hair loss similar to mutations in the Hairless gene.

Radium exposure causes severe health issues, so strict safety measures are essential.

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.

The document emphasizes the importance of correctly identifying and classifying genetic hair disorders to help diagnose related health conditions.

An Indian woman with Short Anagen Syndrome had very short hair and a lower quality of life.

Pregnancy can cause skin darkening, varicose veins, more sweating, hair growth, hair loss after birth, nail changes, and gum inflammation.

Modulating BMP activity changes the number, size, shape, and type of ectodermal organs.

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

Recognizing oral symptoms can help diagnose and treat blood and nutritional diseases early.

Boys with less severe EDA mutations in XLHED have milder symptoms and better sweat and hair production.

The document concludes that there are various treatments for different types of alopecia, but more research is needed for evidence-based treatments.

Hairless mice lack fur due to a genetic mutation affecting skin response, not hormone issues.

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.

Dental erosion is common in adolescents and is linked to diet and higher socioeconomic status.

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.

A 12-year-old girl in Saudi Arabia with Focal dermal hypoplasia showed skin and dental symptoms, highlighting the condition's variability and the need for personalized treatment.

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

Chemotherapy in the first trimester of pregnancy is risky, but in the second and third trimesters, it's generally safe with careful drug selection and timing.