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The study aims to understand the skin and hair characteristics of mothers and their babies, and how these may affect newborns' skin health and mothers' postpartum hair loss.

Researchers created a mouse with the same mutation as humans with trichothiodystrophy, showing similar symptoms and confirming the condition is due to defects in DNA repair and gene activity.

Nanotechnology shows promise for better chronic wound healing but needs more research.

New method finds genetic links between Type 2 Diabetes and Prostate Cancer not seen before.

Children with alopecia areata should only have thyroid screening if they have Down syndrome, a history of atopy, family history of thyroid disease, or signs of thyroid problems.

Some drugs may help treat both COVID-19 and radiation injury.

Different types of cell death affect skin health and inflammation, and understanding them could improve treatments for skin diseases.

Pili torti is a rare condition where hair is twisted and breaks easily, often linked to genetic disorders or other health issues.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.

COVID-19 and vaccines cause various skin reactions and highlight the need for dermatologists in managing these issues and addressing vaccine distribution disparities.

The symposium highlighted the importance of genetics in understanding and treating complex skin diseases.

A TNFAIP3 gene mutation can cause unusual and varied symptoms of lupus and Sjogren's syndrome.

Some COVID-19 patients have different skin problems, which might be the only sign of the virus or related to other health issues.

Miz1 is essential for proper hair structure and growth.

Early diagnosis and tailored treatments are crucial for managing ichthyosis syndromes with hair abnormalities.