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The review shows how to properly diagnose and treat the loss of eyebrow and eyelash hair.

Dermatologists diagnose and manage melanoma more effectively than general practitioners.

A specific enzyme is essential for proper hair follicle stem cell development and healthy skin.

The document is a detailed medical reference on skin and genetic disorders.

Foam corticosteroid covers as well as traditional forms.

sPLA2-IIE is crucial for normal hair follicle structure and skin health.

TGase 3 helps build hair structure by forming strong bonds between proteins.

Phospholipase A2 enzymes play key roles in skin health and disease.

TGM3 is important for skin and hair structure and may help diagnose cancer.

Transglutaminase activity is important for skin and is found in both mammals and birds.

Different genes are active in dogs' hair growth and skin, similar to humans, which helps understand dog skin and hair diseases and can relate to human conditions.

Protein profiling of forehead skin can help distinguish between frontal fibrosing alopecia and androgenetic alopecia.

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

Cholesterol sulfate buildup due to a genetic mutation disrupts the skin barrier, leading to the scaling skin seen in X-linked ichthyosis.

Gene therapy shows promise for treating skin disorders and cancer, but faces technical challenges.

Oral retinoic acid effectively treated collodion baby, with hair loss as the main side effect.

A gene called Gk5 controls lipid production in the skin and affects hair growth.

Steroidogenic isoenzymes may help improve treatments for common hair loss.

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.

The harlequin ichthyosis mouse mutation causes thick skin and early death, resembling a human skin disorder.

The document describes a rare case of IFAP syndrome, a genetic condition with symptoms of hair loss, light sensitivity, and scaly skin.

Melanoma risk tools need improvement, a gene mutation causes a hair disorder that might be treated by managing cell stress, a potential therapy for a skin-ear disorder involves blocking cell channels, skin wrinkling may indicate lung aging regardless of smoking, and oxidative stress might contribute to common baldness.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

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.

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

Genetic testing is crucial for diagnosing congenital atrichia, a rare condition causing irreversible hair loss.

The document concludes that the girl's hairlessness is likely inherited from her parents.

A girl with Netherton syndrome was able to eat wheat without allergies after a special treatment.

Netherton Syndrome is a non-treatable genetic disorder in children causing skin, hair, and allergy issues.