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New ABCA12 gene mutations were linked to a skin condition with scaling and hair loss, and a treatment helped with hair loss in a related case.

Newborns with ichthyosis need specific care based on their skin type.

Mice with the 'lanceolate hair' mutation have abnormal hair and skin similar to human Netherton's syndrome.

Glucosylceramides are essential for healthy skin and proper wound healing.

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

A specific gene mutation (Y449H in K10) was found in a patient with severe skin disorder.

Mutations in keratin genes cause cell fragility and various skin disorders.

A rare skin disorder, Ichthyosis with confetti, has no cure but treatment focuses on managing symptoms with moisturizers.

An 82-year-old man's white hair regained color after taking etretinate for psoriasis.

The Lanceolate hair-J mutation in mice mimics human hair disorders like Netherton's syndrome.

Treatment with moisturizers improved the skin condition of a girl with a rare genetic skin disorder.

Netherton syndrome can cause severe dehydration, infections, and growth issues in infants.

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

Topical minoxidil may not improve the appearance of balding men, according to a letter in this document.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

Mice lacking Insig proteins had hair growth problems due to cholesterol buildup, but this was fixed by the drug simvastatin.

People with late-stage HIV-1 often experience a specific type of hair loss linked to multiple factors, including nutritional issues and immune responses.

Low-potency steroids can cause serious side effects in people with skin conditions like Netherton syndrome.

Most hair loss in children is caused by a few common conditions, and it's important to diagnose these properly and support the child's mental health.

The document concludes that hair loss is common and can be treated with medications like minoxidil or surgical options, and it significantly affects people's psychological well-being.

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

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

Skin's epithelial stem cells are crucial for repair and maintenance, and understanding them could improve treatments for skin problems.

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

Acitretin helped improve hand mobility and skin condition in a patient.

Low IGF-1 and high HDL cholesterol levels are linked to more hair loss in middle-aged women.

The top research priorities for congenital ichthyosis include long-term side effects of oral retinoids, best topical treatments, and treatments for itch and hair loss.

The skin protects the body, regulates temperature, senses touch, and makes vitamin D.

Understanding skin structure and development helps diagnose and treat skin disorders.

Cornification is the process where living skin cells die to create a protective barrier, and problems with it can cause skin diseases.