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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.

Six genetic conditions are often linked to complete scalp hair loss in children.

Wounds on the face usually heal with scars, but understanding how some wounds heal without scars could lead to better treatments.

A new method using bands and finger sheaths from gloves to manage hair during surgery is effective, quick, and reduces hair damage.

Premature hair graying in the face may be influenced by genetics and environment.

Combining microsurgery with craniofacial reconstruction improves aesthetic results and reduces harm to the area where tissue is taken from.

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

Mouse Scube3 affects teeth, tongue, vibrissae, and eye development, but not facial structure or limb growth.

Caspases are enzymes important for both cell death and various non-lethal cell functions, affecting head development and hair growth, with different caspases playing specific roles.

Fish teeth and taste bud densities are linked and can change between types due to shared genetic and molecular factors.

The article concludes that cranial reconstruction should aim for the best aesthetic result, using various techniques tailored to individual needs and conditions.

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.

Msx and Dlx genes are crucial for development, controlling cell behaviors like growth and differentiation through their roles as gene regulators.

Low TRPS1 expression in skin and hair cells is linked to hair problems in Trichorhinophalangeal syndrome.

Basonuclin 2 is vital for the development of facial bones, hair follicles, and male germ cells in adult mice, and its absence can lead to dwarfism and abnormal follicles.

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

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

JAGGED1 could help regenerate tissues for bone loss and heart damage if delivered correctly.

A boy with Oculodentodigital syndrome had a unique GJA1 gene mutation causing his symptoms.

Shrunken heads retain some facial features and hair characteristics, allowing for limited individual identification.

Rat whisker cells can help turn other cells into nerve cells and might be used to treat brain injuries or diseases.

The book "Plastic Surgery, 2nd Edition" is a valuable, comprehensive resource for plastic surgeons.

The 2018 ISPAN Meeting emphasized hands-on learning, patient safety, and professional growth in medical aesthetics and reconstructive practices.

The document says that treating burns late focuses on improving function, appearance, and helping patients return to normal life, using both non-surgical and surgical methods.

Hair pattern in androgenetic alopecia overlaps with scalp and bone demarcations, with distinct gene profiles affecting susceptibility.

Hair follicle transplantation can hide scars but often needs more than one surgery for better results.

Botulinum toxin-A reduces wound and skin graft contraction.

Early surgical removal of scalp hemangiomas leads to good scarring and hair growth.

Hair transplant surgery successfully restored a boy's moustache hair on a cleft lip scar, with natural-looking results and patient satisfaction.

Cerament effectively corrected forehead irregularities in one patient, and various surgical techniques successfully reconstructed perioral soft tissue in 14 patients.