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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.

Oral alitretinoin is effective for certain types of chronic hand eczema, with mild side effects.

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

A patient with PPP had rare skin reactions to adalimumab, which improved after stopping smoking and continuing acitretin.

Focal palmoplantar callosities may help diagnose non-Herlitz junctional epidermolysis bullosa.

Erosive palmoplantar lichen planus in North-East India mainly affects the feet and often involves nails, with unique inflammatory skin changes.

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.

Smoking and certain health conditions like thyroid disease may make palmoplantar pustulosis harder to treat.

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

Olmsted syndrome can be inherited as an autosomal recessive trait due to a rare TRPV3 gene mutation.

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

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

KFSD can be linked to acne keloidalis nuchae and tufted hair folliculitis.

A new gene mutation linked to KID syndrome was found, expanding genetic knowledge.

Etretinate was effective for certain skin conditions, but caused side effects like chapped lips, dry mucous membranes, and hair loss.

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

TRPV3 gene mutations cause Olmsted syndrome symptoms, but severity varies.

The combination of encorafenib and binimetinib caused few skin issues.

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.

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 rare genetic deletion in the KRT1 gene causes unique skin symptoms in a family.

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

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