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A specific gene variant causes severe skin issues and increases infection risk, requiring careful medical monitoring.

Retinoids are effective for various skin conditions and hair loss but have serious side effects, so low doses are recommended.

Two mouse mutants have defective hair cuticle cross-linking.

Acitretin is effective for severe skin conditions but has significant side effects and requires careful monitoring.

Using animal names for skin conditions helps with learning and memory.

Vitamin D is important for skin health and can help treat psoriasis, atopic dermatitis, and vitiligo.

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

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

A specific gene mutation causes Olmsted syndrome.

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

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.

About 12% of children in Kota, Rajasthan, experience hair loss, mainly due to fungal infections, with early treatment advised to prevent worsening.

Understanding keratinization is crucial for treating skin conditions like ichthyoses and psoriasis.

Using powdered umbilical remnant allograft can effectively treat chronic scalp wounds resistant to traditional treatments.

Topical corticosteroids are the main treatment for Erosive Pustular Dermatosis, but recurrence is common after stopping treatment.

Foam corticosteroid covers as well as traditional forms.

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

Understanding the genetics of rare inherited ichthyosis syndromes is key for better treatments and genetic counseling.

A Brazilian male with IFAP syndrome has a unique genetic variant causing his condition.

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

A new gene mutation linked to a skin condition was found in a Spanish family.

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

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

A baby was diagnosed with IFAP syndrome due to a new genetic mutation, showing severe skin and developmental issues.

Ichthyoses are skin disorders causing scales, with treatment depending on type and severity.

The skin is a complex barrier that protects the body, regulates temperature, and helps with immune responses.

ESR2 gene linked to female-pattern hair loss.

TCDD speeds up skin barrier formation by increasing certain gene expressions.