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A rare genetic skin condition usually affecting males was found in a 9-year-old girl.

A new gene mutation linked to Olmsted syndrome may increase cancer risk, suggesting the need for ongoing patient monitoring.

A man with KID syndrome developed a rare cancer in a long-term skin infection.

Connexin-26 gene mutations may increase cancer risk in KID syndrome patients.

Ruxolitinib significantly improves multiple autoimmune conditions in APS-1 patients.

Higher hs-CRP levels in Indian adolescent women with PCOS are more related to BMI than PCOS itself.

A rare genetic disease caused severe, worsening hair loss from early childhood with poor treatment results.

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.

Bardet-Biedl syndrome may include under-recognized skin problems related to its metabolic disturbances.

A woman with a specific mutation causing adrenal gland issues faced fertility problems, but careful hormone therapy helped her manage it successfully.

The woman likely has secondary syphilis, treatable with penicillin.

Older men's scalp damage increases with age and sun exposure, a baby girl in the Philippines has Schimmelpenning syndrome, and thyroid screening is advised for children with hair loss and certain risk factors.

A boy with alopecia regrew hair using a vitamin D cream after other treatments failed.

Early exposure to fluoride, lead, and certain nutrients affects puberty differently in boys and girls.

Oestrogens are key for bone growth during puberty in both boys and girls.

Baicalin may help treat severe drug-induced skin reactions.

A newborn with severe low blood sugar due to a genetic issue needed major surgery after standard treatments failed.

NISCH syndrome is a rare genetic disorder affecting skin and liver, with variable symptoms and limited treatment options.

Hair casts, also called pseudonits, are often mistaken for other conditions.

A boy with chromosome 13q deletion syndrome developed eye cancer, a woman with breast cancer lost vision due to a rare side-effect of her treatment, a man's vision worsened after using a hair loss drug, and two rare disorders were discussed. Optical Coherence Tomography is useful for diagnosing and monitoring these conditions.

Changing protein kinase levels in pituitary cells affects calcium flow and beta-endorphin release.

A girl with Becker's nevus syndrome showed good improvement in breast development using spironolactone.

Certain genetic variants reduce enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

If someone has scaly skin, muscle stiffness, and intellectual disability, doctors should consider Sjogren-Larsson Syndrome, but other conditions if more symptoms are present.

Deleting vitamin D and calcium receptors in skin cells increases skin cancer risk by reducing DNA repair and stress response.

Blocking the JAK/STAT pathway may help reduce skin sensitivity in Xeroderma pigmentosum.

Excessive iodine from a cystic fibrosis supplement can cause hypothyroidism.

The document reports the first case of a rare skin condition in Colombia, the 19th case worldwide.

Kids with alopecia areata had lower vitamin D levels than healthy kids.

Cyclophosphamide likely causes skin darkening by affecting hair follicles.