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Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

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

The document concludes that unruly hair can be congenital or acquired, often lacks specific treatments, and can be managed with oils and short hairstyles.

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.

Researchers made a mouse model with curly hair and hair loss by editing a gene.

The 2015 Hair Research Congress concluded that stem cells, maraviroc, and simvastatin could potentially treat Alopecia Areata, topical minoxidil, finasteride, and steroids could treat Frontal Fibrosing Alopecia, and PTGDR2 antagonists could also treat alopecia. They also found that low-level light therapy could help with hair loss, a robotic device could assist in hair extraction, and nutrition could aid hair growth. They suggested that Alopecia Areata is an inflammatory disorder, not a single disease, indicating a need for personalized treatments.

Some congenital hair disorders improve in childhood or with treatments like minoxidil and retinoids, while others like Netherton syndrome and trichothiodystrophy have a poor prognosis.

To diagnose hair loss, use a systematic approach including history, exams, and tests.

Hair shaft disorders, often due to genetics or environment, lack specific treatments but can be managed with gentle hair care and may improve with age or topical treatments.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

The enzymes Tet2 and Tet3 are important for skin cell development and hair growth.

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

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

A mutation in the FAM83G gene is linked to skin and hair abnormalities in two related individuals.

Children's hair loss can be caused by many factors, including autoimmune diseases, emotional stress, genetics, and infections, with treatment and prognosis varying.

Bald thigh syndrome in sighthounds is caused by structural defects in hair shafts due to downregulated genes and proteins.

The document concludes that proper diagnosis and management of hair loss in children require a detailed examination and understanding of various hair disorders.

The most common cause of hair loss in children is tinea capitis, followed by alopecia areata and telogen effluvium.

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

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

New treatments targeting specific genes show promise for treating keratin disorders.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

The document concludes that early diagnosis and a comprehensive treatment plan are crucial for managing hair loss in children, with a focus on both medical and psychological support.

Some domesticated animals have the same genetic skin diseases as humans, which can help doctors understand human genetic mutations.

The guide helps doctors diagnose hair problems by suggesting a thorough patient history, physical exams, and various diagnostic tools.

The document concludes that accurate diagnosis and understanding the type of hair disorder are crucial for treating hair loss in children.

The document concludes that understanding hair biology and recognizing hair conditions are crucial for managing and treating hair loss in children.

The HOXC13 gene affects different hair proteins in cashmere goats in varied ways and is controlled by a feedback loop and other factors.

Eyebrow loss has many causes and requires accurate diagnosis for proper treatment.