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A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.

Understanding normal hair growth and loss in children is key to diagnosing and treating hair disorders.

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

The article explains the genetic causes and symptoms of various hair disorders and highlights the need for more research to find treatments.

Genetic mutations can cause hair growth disorders by affecting key genes and signaling pathways.

The document explains the genetic causes and characteristics of inherited hair disorders.

Rabbits lacking the Hoxc13 gene show similar hair and skin issues to humans with ECTD-9, making them good for research on this condition.

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

The document concludes that early diagnosis and treatment are crucial for children with hair loss to prevent permanent damage, although not all conditions can be effectively treated.

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

The document concludes that over 500 genes are linked to hair disorders and this knowledge is important for creating new treatments.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

The document concludes that periocular hair disorders have various causes and treatments, and proper evaluation by specialists is important for management and prognosis.

Terbinafine is more effective than itraconazole for toenail fungus, especially in older patients, and debridement improves its effectiveness.

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.

Trichoscopy is a useful tool for diagnosing hair disorders without pulling out hair.

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

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

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

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

The document concludes that mouse models are crucial for studying hair biology and that all mutant mice may have hair growth abnormalities that require detailed analysis to identify.

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

Hair problems can be caused by genetics or the environment, and treatment should focus on the cause and reducing hair damage.

Poliosis circumscripta is a patch of white hair caused by lack of melanin, linked to genetic and acquired conditions.

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

Bimatoprost is effective for growing longer, thicker, and darker eyelashes.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

Uncombable hair syndrome causes frizzy hair and can affect the nervous system, eyes, and ears, often co-occurring with other hair, skin, nail, and teeth conditions, and is linked to three specific gene mutations.

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