Search

everythinglearnresearchcommunity

for

Search:↓

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.

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

A specific gene mutation causes vitamin D resistance, but certain vitamin D analogs might help.

CE-PTG detects early hair follicle issues in balding areas, helping measure male hair loss.

Two siblings with a genetic mutation had a form of rickets that doesn't respond to vitamin D.

Different scalp imaging methods are important for studying hair and scalp health and require more volunteers for better evaluation.

Hirosaki hairless rats lack hair due to missing DNA with key keratin genes.

A new mutation in the Hr gene causes hair loss in mice, similar to a human hair disorder.

A new method effectively visualizes keratin in hair without harsh chemicals.

Translucent keratin films are better for testing hair dyes.

The hairless gene mutation causes baldness by disrupting hair follicle structure.

CAH is a genetic disorder affecting cortisol production and causing hormonal imbalances, with treatment and diagnosis varying by form and symptoms.

Ionizing radiation damages human hair follicles by stopping cell growth, causing cell death, disrupting color, and increasing stress and damage markers.

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

The enzyme RDH12 plays a role in vision and retinal disease, with mutations leading to early onset visual loss and blindness, but the exact disease mechanism is unclear and there are no treatments yet.

Hereditary elliptocytosis causes elongated red blood cells and can lead to mild or no symptoms.

Thermal imaging is a useful non-invasive method to diagnose active inflammation in frontal fibrosing alopecia.

Three siblings with a genetic form of rickets showed different symptoms of the disease.

Screening for iron levels in patients with hair loss may help find a genetic iron overload condition early.

In vivo reflectance confocal microscopy is useful for evaluating hair shaft diseases but needs improvement for deeper hair follicle issues.

Hair cortisol measurement can help diagnose and monitor Cushing’s disease.

Permanent wave treatment with thioglycolic acid changes hair structure by altering disulfide bonds.

Shh and Dhh affect skin development and can cause tumors, while Ihh does not.

Natural hair is a return to its original state, while modifications signal social pressures.

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

The DWLSM provides detailed imaging of hair shafts and follicles with high accuracy.

A black-skinned woman was diagnosed with Vogt-Koyanagi-Harada disease and treated with steroids and eye drops.

High insulin levels may increase the risk of pilonidal sinus disease in female teens.