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A Chinese family had a child with a specific gene mutation causing vitamin D-resistant rickets, but the child improved with calcium and low-dose calcitriol.

Early and accurate diagnosis is crucial for managing rare genetic disorders like this localized variant of junctional epidermolysis bullosa.

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The G allele of IFITM3 rs12252 is linked to more severe COVID-19.

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DKK4 can be used to improve wool quality in Zhexi Angora rabbits.

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DS-2325a is safe and well-tolerated, supporting further development for Netherton Syndrome treatment.

The PCR technique can identify genetic differences in a wool-related gene among different sheep breeds, which may help improve wool and pelt quality.

A new gene mutation causes vitamin D-resistant rickets and hair loss in two siblings.

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This is a schedule of hair restoration surgery events.

This is a schedule of hair restoration surgery events.

This is a schedule of hair restoration surgery events.

This is a schedule of hair restoration surgery events.

This is a schedule of hair restoration surgery events.

This is a schedule of hair restoration surgery events.

KRT14 gene variants cause dermatopathia pigmentosa reticularis, affecting nails, teeth, and hair.

The method accurately measures Finasteride and Tamsulosin in tablets without interference.

The new synthetic retinoid RO 13-6298 effectively treated severe psoriasis at low doses with manageable side effects.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

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

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

China approved Sinovac's flu vaccine, Japan approved RiUP for female hair loss, and Nippon Kayaku's three cancer drugs.

PF-998425 is a new, effective, and non-phototoxic treatment for skin conditions related to androgens.

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The IBHRS is now operational.