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sPLA2-IIE is crucial for normal hair follicle structure and skin health.

Phospholipase A2 enzymes play key roles in skin health and disease.

Genetic changes in mice help understand skin and hair disorders, aiding treatment development for acne and 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.

Oral isotretinoin temporarily improved skin symptoms in a child with IFAP syndrome.

Environmental factors can cause mutations in skin proteins, leading to skin disorders.

Long-term use of finasteride and dutasteride can cause serious health issues like diabetes and liver problems.

A calf in Scotland likely had Schmallenberg virus from its mother.

A specific gene mutation causes Olmsted syndrome.

Three related Persian cats have a rare, likely hereditary skin condition causing hair loss and poor coat quality, with limited treatment options.

Efficient delivery systems are needed for the clinical use of CRISPR-Cas9 gene editing.

Topical ceramide treatment partially improves the skin condition in Jack Russell Terriers with a genetic skin disorder.

Netherton's syndrome is linked to high IgE levels and unique skin and hair symptoms, and may improve with ammonium lactate lotion and allergy management.

The document reports unique growth lines in a child after Stevens-Johnson syndrome, skin reaction from parsnips and sun in a girl, and itchy skin with xanthomas in a boy with Alagille syndrome.

The document concludes that the exact way alcohol causes harm to fetal development is unknown, but it significantly affects nutrient transport to the fetus and a safe level of alcohol during pregnancy is not determined.

The document concludes that accurate diagnosis of ichthyosis is crucial for treatment and genetic advice, and ongoing research is needed for better therapies.

Zinc is crucial for nutrition, especially in patients with specific health conditions, and requires careful supplementation and monitoring.

Inherited ichthyoses cause widespread skin scaling and thickening due to gene mutations.

Gonadal dysgenesis, like Turner's and Klinefelter's syndromes, negatively affects bone health, but hormone treatments can help.

Scarring alopecias are complex hair loss disorders that require early treatment to prevent permanent hair loss.

The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

The most common causes of hair loss in children in South-East Nigeria are fungal infections and alopecia areata.

The document concludes that hair loss in cats is caused by various factors, including allergies, mites, infections, and hormonal issues, with treatments varying accordingly.

Lymphatic vessels are essential for health and can be targeted to treat various diseases.

Using the right hair care products can improve hair health and help manage hair disorders.

A cross-bred lamb with severe skin and movement issues had ichthyosis fetalis but normal vitamin A levels.

Certain Prakruti types are more prone to early male pattern baldness.

Follicular Unit Extraction (FUE) is a popular hair transplant method with minimal scarring that can transplant many grafts quickly and improve appearance and psychological well-being.

Antioxidants may help improve mitochondrial health and could be used to treat diseases related to cell damage.

Certain factors can start hair growth in adult skin by making cells communicate and form new hair follicles.