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A new mutation in the HJV gene was found in a young woman with juvenile hemochromatosis, causing unusual symptoms like secondary hypothyroidism.

New method, hair distribution width (HDW), improves accuracy in diagnosing androgenetic alopecia (AGA).

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.

pdHGF speeds up wound healing and hair growth.

Growth hormone therapy can improve symptoms and growth in children with Vitamin-D Dependent Rickets Type-2.

Mutations in the vitamin D receptor cause hereditary vitamin D-resistant rickets, leading to poor bone health and requiring high calcium doses for treatment.

Hoyeraal-Hreidarsson syndrome in infants causes severe gastrointestinal issues.

A man had two rare autoimmune diseases that might be connected.

Cinacalcet may help treat hereditary vitamin D resistant rickets safely.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

These hair loss conditions might be part of a spectrum, not separate issues.

Recombinant human growth hormone helps burn wounds heal faster by increasing blood vessel growth.

The modified stem cells with VEGF165 in a special scaffold improved blood vessel growth and wound healing for skin repair.

A vitamin D receptor mutation causes rickets and affects immune responses.

A new genetic mutation linked to Hutchinson-Gilford progeria syndrome was found in China.

HGF combined with ADA is highly accurate for diagnosing tuberculous pleural effusion, especially in younger females.

Early diagnosis and aggressive treatment are essential for managing Vogt-Koyanagi-Harada syndrome effectively.

Hutchinson-Gilford Progeria Syndrome caused rapid aging due to a genetic mutation, with treatments to manage symptoms.

Skin changes help detect graft-versus-host reaction early after bone marrow transplants.

The Hair Diameter Index (HDI) was created to help plan hair restoration surgery after finding that visual hair density is linked to hair count and thickness, not volume.

A boy with Oculodentodigital syndrome had a unique GJA1 gene mutation causing his symptoms.

New mutations in the VDR gene cause vitamin D-resistant rickets without hair loss.

Intravenous calcium therapy is a safe and effective treatment for a rare type of rickets.

Hutchinson-Gilford Progeria Syndrome causes rapid aging due to a gene mutation, with no cure yet, but research may lead to better treatments.

Researchers created a mouse model of a type of rickets that does not cause hair loss.

HVDRR is caused by VDR gene mutations, leading to vitamin D resistance, treatable with high calcium doses, but alopecia remains permanent.

Early treatment with corticosteroids improved her eye condition significantly.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

A genetic mutation in the CDH3 gene causes hair loss and vision problems in a young Saudi girl.

A deletion in the CDH3 gene causes a rare disorder with short hair and vision loss.