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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.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

Platelet-rich Plasma (PRP) helps treat hair loss effectively, especially when prepared using the double-spin method.

The document concludes that skin biopsies, genetic and environmental factors, and specific treatments are important in managing cutaneous lupus erythematosus.

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

Taking vitamins, minerals, and amino acids can improve hair strength and quality in people with Monilethrix.

The document concludes that accurate diagnosis of ichthyosis is crucial for treatment and genetic advice, and ongoing research is needed for better therapies.

Using gelatin sponges for deep skin wounds helps bone marrow cells repair tissue without scarring.

Drug repositioning offers hope for new, affordable treatments for a genetic skin disorder called ARCI.

Female mice with disrupted 5α-reductase 1 had significant metabolic issues, including stress response problems, insulin resistance, liver fat buildup, and obesity.

The 2004 hair research meeting presented new findings on hair cell differentiation, genetic factors in hair loss, hair pigmentation, and potential targeted therapies.

A potential treatment for atopic dermatitis could be to increase PADI1 expression to improve skin barrier function.

A girl with skin rashes and low zinc levels improved with zinc supplements and had new gene mutations linked to her condition.

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.

The rhg mutation in mice affects the Oat gene, causing hair growth issues and other symptoms.

A 72-year-old man was diagnosed with a rare skin form of Rosai-Dorfman disease after years of misdiagnosis.

People with Birt-Hogg-Dubé syndrome often have lung problems and delayed diagnosis, and better recognition of CT scan signs could improve diagnosis and management.

The study found that the hair loss condition in Cesky Fousek dogs is influenced by multiple genes affecting skin and muscle structure, fat metabolism, and immunity.

Human Schwann cells can be quickly made from hair follicle stem cells for nerve repair.

The study found that alopecia areata is strongly linked to autoimmune diseases and may indicate a genetic predisposition to such conditions.

MOF controls skin development by regulating genes for mitochondria and cilia.

Researchers developed a cost-effective 66 K SNP chip for cashmere goats that is accurate and useful for genetic studies.

Finasteride and dutasteride may help prevent hair loss but could cause side effects like sexual dysfunction and psychological issues.

Alopecia Areata is an autoimmune disease affecting hair follicles, influenced by genetic and environmental factors, with rodent models being essential for research.

Patterned hair loss in women is linked to hormonal imbalances and biochemical changes, and should be evaluated for underlying health issues.

Polycystic Ovary Syndrome is linked to higher risk of hypertension and heart disease.

Accurate clinical, histological, and genetic methods are key for understanding and treating hair disorders.

Some lesser-known causes of PCOS include autoimmune issues, genetic mutations, and changes in the body's microbiome.

Skin lesions in Carney Complex are caused by a gene change in some skin cells that leads to increased pigmentation and may lead to tumors.

Hair and nails are similar keratin structures with different shapes and growth, affected by the same diseases and environmental factors.