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Dupilumab helped improve skin and prevent new lesions in a child with a rare immune disorder and severe eczema.

The F9 formulation of Finasteride tablets, using Eudragit, successfully controlled drug release.

New genotype linked to non-classical congenital adrenal hyperplasia found in Italian siblings.

All four treatments for early rheumatoid arthritis had similar safety profiles.

Mirvetuximab soravtansine improves quality of life and reduces symptoms more than standard chemotherapy in ovarian cancer patients.

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Polygonum multiflorum is used for health benefits but may cause liver issues.

A new method creates valuable compounds for drug discovery by breaking traditional chemical rules.

CTLA4 gene variants are not linked to alopecia areata in Monterrey's Mexican population.

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Astilbin can potentially calm overactive immune responses, like in Type 1 Diabetes, by suppressing certain cell activities and reducing inflammation.

Oral tacrolimus helped a rheumatoid arthritis patient regrow hair lost due to alopecia areata.

INTASYL is a promising, adaptable RNAi technology for treating skin cancers.

A certain mutation in the fetal alpha 5-reductase gene is linked to a higher risk of late miscarriage.

Rhupus is a complex syndrome that is hard to diagnose due to unclear clinical criteria.

Human adrenals and gonads have a unique enzyme for steroid hormone production.

GRF is not safe for tubal occlusion.

pbn-STAC effectively finds strategies for cellular reprogramming using deep reinforcement learning.

A new genetic mutation causing Xeroderma Pigmentosum was found in an 8-year-old girl, affecting her DNA repair.

The NUDT15 gene variant causes severe side effects from azathioprine in some Indian patients.

The AIRE gene variant rs2075876 is linked to a higher risk of alopecia areata in males.

Certain genetic markers on chromosome 20 are linked to hair loss in the Han Chinese from Yunnan.

The discovery of 5α-reductase deficiency in guevedoces led to the development of important urologic medications.

Double-stranded RNA activates a pathway that causes a skin protein to be expressed in the wrong place.

A KLK5 inhibitor effectively improved skin symptoms in a mouse model of Netherton Syndrome.

Certain genetic changes in the KRT82 gene may cause patchy skin in New Zealand rabbits.

The UD-PrOZA program successfully diagnosed 18% of adult patients with rare diseases, often using genetic testing.