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A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

A girl with a rare skin condition improved after one month of treatment with acitretin.

Topical 6% salicylic acid effectively reduced skin plaques in a patient with wooly hair and palmoplantar keratoderma.

A patient got a skin reaction on their hands and feet after using secukinumab for psoriasis.

People with palmoplantar pustulosis, especially with bone issues, have different mouth bacteria compared to healthy people.

Nagashima-type palmoplantar keratosis in Asians is caused by a SERPINB7 gene mutation.

Carbamazepine caused hair loss and skin eruptions in a woman, which improved after stopping the medication.

The woman was diagnosed with lichen sclerosus, a rare skin condition, after initial misdiagnosis and ineffective treatments.

Excimer light effectively treats various skin diseases, including psoriasis, vitiligo, and mycosis fungoides.

Ice-skating athletes often have skin problems due to cold, infections, and inflammation, needing careful treatment and prevention.

Understanding genetic mutations helps diagnose and treat skin disorders like ichthyosis.

Smoking harms skin health, causing slower wound healing, more wrinkles, and worsening some skin conditions, but may protect against certain others.

WNT10A mutations cause varied symptoms in patients with odonto-onycho-dermal dysplasia.

New genes linked to woolly hair have been found, which could help treat it and change hair texture.

Pityriasis rubra pilaris significantly worsens quality of life more than many other health conditions.

PRP patients show varied symptoms and need more research to understand related conditions.

Dermatopathia pigmentosa reticularis causes skin discoloration, hair loss, and nail problems.

Papillon-Lefèvre Syndrome causes early tooth loss and skin issues, needing early dental diagnosis.

Patients on dabrafenib and trametinib for melanoma often experience skin side effects.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

Krt16-deficient mice help understand skin disorders like PC and FNEPPK.

Olmsted syndrome is a rare skin disorder causing thickened skin and other symptoms.

Taking too much vitamin A can cause health problems like bone pain and hair loss.

A Jordanian family with Clouston syndrome has a common GJB6 gene mutation.

Different types of skin on mice have unique chemical profiles related to how they grow and react to stress.

A baby with KID syndrome died from infections and organ failure at 18 months old.

Clouston's syndrome is a rare disorder affecting nails, hair, teeth, and skin, caused by a gene mutation, and currently has no treatment, only supportive care.

New RIPK4 gene mutations were found to cause a type of skin and limb birth defect.

Skin problems are common in thyroid disorders, with dry skin in hypothyroidism and warm, soft skin in hyperthyroidism.

The chapter explains that there are many genetic skin disorders affecting skin cell formation, including both common and rare types.