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IVIG therapy significantly improved symptoms in a patient with APS-2 and SPS.

DDS treatment for LABD can cause severe side effects like anemia and hair loss, requiring careful monitoring.

A cat's poor wound healing was linked to a genetic deletion in the COL5A1 gene.

Cefazolin-loaded nanoparticles in nanofibers can help heal wounds and support regeneration.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

Children and adults with Cushing's disease show different symptoms and males have more severe cases; surgery outcomes can be predicted by certain factors.

A new fluorescent material can detect dextran sulfate sodium, turning green when present, useful for forensic and environmental monitoring.

A 15-year-old girl with no menstrual period was diagnosed with a genetic condition that makes her body unable to respond to male hormones, leading to female characteristics despite having male genetic makeup.

The gene for Clouston syndrome in a large Indian family is located in the 13q11-q12.1 region.

Cadd4 effectively reduces cholesterol levels without side effects.

Cabergoline helped a boy with Cushing disease get better after surgery and radiotherapy didn't work.

MCTD should be considered in children with recurring muscle issues, lupus-like symptoms, and edema.

Non-drug methods effectively managed agitation in a patient with a heart device, leading to improved mental function.

Skin organoids with NCSTN mutation show changes in hair follicle development and higher inflammation, key features of Hidradenitis Suppurativa.

Nrf-2-modified stem cells from hair follicles significantly improve ulcerative colitis in rats.

A woman developed severe bladder inflammation after cancer treatment with Cytoxan.

Syndecan-1 is essential for maintaining skin fat and preventing cold stress.

Skin tumors with CYLD cutaneous syndrome show more NF-κB activity and less organized collagen.

Ketoconazole improved symptoms of ACTH-independent Cushing syndrome despite inconclusive initial scans.

CRPS type I is a complex pain condition with no proven cure, requiring personalized treatment.

A 12-year-old boy with PAIS successfully developed male characteristics using high-dose testosterone and anastrozole.

The compound (NH4)2Mn0.17Cu0.83Cl4.2H₂O has a specific structure, shows weak magnetism at low temperatures, and undergoes phase changes at high temperatures.

The hydrogel quickly stops bleeding and helps heal infected wounds.

In Japan, sex reassignment surgery for gender identity disorder faces challenges and needs better medical support and education.

Surgical excision is the best treatment for SCC, but intralesional cidofovir might be a viable alternative.