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Dermoscopy improves diagnosis and treatment monitoring for children's skin infections, inflammations, and hair disorders.

The conclusion is that exogen is a unique hair cycle phase and the new sampling method specifically targets this stage, which may help in future hair loss research.

Smad4 is important for healthy hair follicles because it helps produce a protein needed for hair to stick together and grow.

Genetic research has advanced our understanding of skin diseases, but complex conditions require an integrative approach for deeper insight.

A gene deletion in mice causes weak protein, immune issues, hair loss, airway problems, and wasting disease.

The review highlights the importance of stem cells in hair health and suggests new treatment strategies for hair loss conditions.

Photodynamic therapy may not work for erythroplasia of Queyrat and could lead to invasive squamous cell carcinoma.

Cats with abnormal hair had DSG4 gene changes causing hair problems.

HOXC13 is essential for hair and nail development by regulating Foxn1.

Desmoglein 4 is controlled by specific proteins that affect hair growth.

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

Hair microscopy is a simple and cost-effective method to help diagnose systemic diseases in children.

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

Lipase H is important for hair follicle function and shaping hair fibers.

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

Marie-Unna Hereditary Hypotrichosis is a rare genetic condition causing sparse hair growth, requiring specific recognition for proper care.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

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

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

The conclusion is that genetic testing is important for diagnosing and treating various genetic hair disorders.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

Different skin diseases show unique patterns of skin cell separation, cell death, and granular layer changes.

New LPA receptors (LPA4, LPA5, LPA6) have diverse roles in the body.

Cholesterol balance is important for hair health, and problems with it can lead to hair loss conditions.

Diagnosing alopecia areata is challenging and requires careful examination and various tests to distinguish it from other hair loss types.

Mice with extra human KLK14 had hair and skin problems, including weaker cell bonds and inflammation, linked to Netherton syndrome.

Bone marrow stem cells and their medium help hair regrowth.

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

P-cadherin is important for hair growth and health, and its problems can cause hair and skin disorders.

Applying minoxidil can help improve hair growth in people with hair loss caused by LIPH gene mutations.