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The FGF5 gene variant causes long hair in Akitas, and genetic testing is advised to manage coat length and welfare.

Longer TA repeats in the SRD5A2 gene may increase acne risk in Chinese people.

The new FUE device improves hair transplant safety and efficiency.

Dietary L-serine supplementation can reduce symptoms of HSAN1 by lowering harmful 1-deoxySL levels.

Nagashima-type palmoplantar keratosis in Asians is caused by a SERPINB7 gene mutation.

Adding dutasteride to therapy may improve treatment for advanced salivary duct cancer.

Turkish Van cats' genotypes don't affect traits like eye color or hair length.

Connexin-26 gene mutations may increase cancer risk in KID syndrome patients.

Cone beam computed tomography can allow for smaller safety margins around the target area in prostate cancer radiation treatment if used for ongoing treatment checks.

Certain genetic variants may increase the risk of developing PCOS.

Variegated coat color in cats is linked to the Silver locus.

A new mouse mutation causes skin and hair defects due to a gene change.

Certain gene variants may raise the risk of prostate enlargement, but taking NSAIDs could reduce this risk.

A new mutation in the STS gene causes X-linked ichthyosis, even in rare female cases.

A multidisciplinary approach is crucial for managing Silver-Russell syndrome effectively.

A heterozygous mutation in HTRA1 can cause severe CARASIL symptoms.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

Cantú syndrome may be linked to pituitary adenomas.

ETS2 drives cancer progression in squamous cell carcinoma and is linked to poor patient outcomes.

Tanning ability is linked to specific DNA changes in skin genes.

Tangent screens help detect visual field defects from vigabatrin.

The nicotinamide supplement did not reduce symptoms in horses with insect bite hypersensitivity.

Scalp basal cell carcinoma in Asians is different from facial basal cell carcinoma, with unique features like being more common in younger people and having larger tumors.

Tebentafusp-tebn improves survival rates in uveal melanoma patients but has common side effects like rash and fatigue.

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

The NUDT15 R139C variant causes thiopurine-induced leukocytopenia through a different mechanism than previously thought in Japanese patients with inflammatory bowel disease.

A reliable method was developed to measure candesartan in human plasma.

The TRPV3 gene variant may cause the long-haired suri alpaca coat.

Clouston syndrome is inherited in an autosomal dominant pattern and caused by a specific gene mutation, with no current treatment available.