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

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

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

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

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

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

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

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

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

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

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

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

Chemotherapy successfully treated both Hodgkin's disease and skin lesions.

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

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

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

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

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

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

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

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.

Two cycles of ABVD chemotherapy followed by 20 Gy radiotherapy is the new standard for early-stage Hodgkin lymphoma due to lower toxicity and similar effectiveness.

Suppressing the HGPS mutation may improve symptoms and suggest reversibility.

A woman with childhood growth hormone deficiency had multiple hormone deficiencies and developed serious lung and kidney problems later in life.

A new gene mutation causes vitamin D resistance and rickets, treatable with calcium therapy.

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

Women with excessive hair growth or polycystic ovary disease may more often carry a gene variant for 21 hydroxylase deficiency.

The R343H mutation in the VDR gene causes vitamin D-resistant rickets with alopecia by impairing specific gene activity.

Mutating the gmds gene in zebrafish increases hair cell numbers and regeneration.

A rare genetic disorder causes sparse hair and vision loss due to a CDH3 gene mutation.