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

TGM3 is important for skin and hair structure and may help diagnose cancer.

The study found key factors in the cause of hidradenitis suppurativa, its link to other diseases, and identified existing drugs that could potentially treat it.

Different types of cell death affect skin health and inflammation, and understanding them could improve treatments for skin diseases.

Transglutaminase activity is important for skin and is found in both mammals and birds.

Different genes are active in dogs' hair growth and skin, similar to humans, which helps understand dog skin and hair diseases and can relate to human conditions.

Protein profiling of forehead skin can help distinguish between frontal fibrosing alopecia and androgenetic alopecia.

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.

Lash ptosis is more common and severe in people with congenital eyelid droop than in those with acquired eyelid droop or without eyelid droop.

Madarosis is the loss of eyelashes and eyebrows due to various health issues and requires thorough examination to diagnose and treat the underlying cause.

Oral retinoic acid effectively treated collodion baby, with hair loss as the main side effect.

Psoriasis is the most common cause of erythroderma, and proper medical follow-up is crucial.

The document concludes that understanding hair structure is key to diagnosing hair abnormalities and recommends gentle hair care for management.

Steroid Sulfatase inhibitors show promise in treating hormone-dependent disorders like cancers, hair loss, and acne, with 667COUMATE being a potential candidate for breast cancer treatment trials.

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

A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.

Over half of the dog skin disorders discussed have known gene variants, enabling genetic testing for diagnosis and responsible breeding.

Bovines can have rare inherited skin diseases with specific symptoms like hair loss, fragile skin, and abnormal porphyrin buildup.

The four patients have a unique type of ichthyosis affecting hair follicles.

A Chinese man with KID syndrome had a new mutation in the GJB2 gene.

Mutations in keratin genes cause cell fragility and various skin disorders.

A boy with Sjogren-Larsson syndrome has skin and muscle symptoms due to a specific enzyme deficiency.

A 15-year-old with KID syndrome developed a rare skin condition called PEHFN.

The document describes a rare case of IFAP syndrome, a genetic condition with symptoms of hair loss, light sensitivity, and scaly skin.

Surgery on a baby with a skin disorder improved eyelid position and eye health.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

Some hair loss disorders are caused by genetic mutations affecting hair growth.

A Japanese patient with IFAP syndrome had a severe MBTPS2 gene mutation but showed milder symptoms than previously observed cases.

Minoxidil cream can safely treat hair loss in kids with ectodermal dysplasia.

Acitretin helped improve hand mobility and skin condition in a patient.