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The new FDA labeling rules provide more detailed drug safety information for pregnant and breastfeeding women, but more data is needed on the risks of many dermatologic drugs.

The most common skin problems in perimenopausal women in South India are infections, eczemas, and acne, possibly worsened by external factors and lifestyle practices.

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

The man likely has secondary syphilis affecting his nervous system.

Neonate rabbits have consistent skin layers and no sweat glands.

Most patients with dermatomyositis had skin rash, itching, and muscle weakness, treated mainly with prednisolone and hydroxychloroquine.

The hydrogel patch helps heal diabetic wounds by releasing a healing agent in response to harmful molecules and improving skin regeneration.

A rare genetic disease causes sparse hair and early blindness due to a gene mutation.

A 6-year-old boy's leg hair loss was due to friction from sitting cross-legged, and it usually resolves on its own.

Resident doctors had more facial skin discoloration than medical students during COVID-19.

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

Early diagnosis and a multidisciplinary approach are crucial for children with Trichothiodystrophy and hidden learning disorders.

Newborn acne may be linked to family history of high male hormone levels.

Childhood cancer survivors need better skin care and sun protection.

A new microneedle patch effectively treats atopic dermatitis by reducing skin stress and restoring immune balance.

Current treatments for neutrophilic alopecias in children are limited and often ineffective, especially for males and those of Afro-Caribbean descent.

Dermoscopy quickly and accurately diagnosed a rare hair disorder in a 12-year-old girl.

A new genetic mutation was found causing hair and eye issues in a boy.

Topical treatment is recommended for Folliculitis decalvans in pregnant women.

Brazilian patients with inflammatory bowel disease have a high rate of skin problems compared to healthy people.

A 30-year-old man with rare skin conditions improved with antibiotics and surgery, hinting at a link to rosacea.

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.

Abrocitinib, a JAK inhibitor, may help treat atopic dermatitis and alopecia universalis together.

The patient improved after antiviral treatment for a viral infection.

Anti-Ro exposed children had more reported neuro-psychiatric issues, but differences from healthy controls were not significant.

A rare case of trichothiodystrophy was found with autism, seizures, and mental retardation.

Children with alopecia areata, especially with Down syndrome or thyroid issues, should be screened for thyroid disease.