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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.

Epidermolysis bullosa simplex causes easily blistered skin due to faulty skin cell proteins, leading to new treatment ideas.

Most hospitalized children with skin issues were boys, with allergic skin diseases like atopic dermatitis being most common, and treatments were usually topical.

The document concludes that treating skin conditions should include psychological care and a multidisciplinary approach is essential for effective management.

The document discusses various skin disorders and new therapeutic approaches.

Two boys had a rare skin condition needing to be differentiated from similar disorders, with unclear inheritance due to few cases.

Newborns with ichthyosis need specific care based on their skin type.

Understanding the genetics of rare inherited ichthyosis syndromes is key for better treatments and genetic counseling.

Acitretin moderately improved skin and eye issues but not hair loss or light sensitivity in a 3-year-old with IFAP syndrome.

A mother and daughter had severe skin, hair, and eye issues linked to IFAP.

Children with severe ichthyosis and growth failure rarely have nutritional deficiencies or gastrointestinal issues, but may experience chronic dehydration.

Ichthyosis with confetti is a genetic skin disorder with consistent ectodermal malformations and various KRT10 gene mutations.

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

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

Balneophototherapy effectively treats ichthyosis linearis circumflexa but may need ongoing treatment due to short remission.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

Narrowband UVB therapy significantly improved a child's rare skin condition.

A rare skin disorder, Ichthyosis with confetti, has no cure but treatment focuses on managing symptoms with moisturizers.

A rare skin condition with dark, thick, warty patches and some hair loss was found in a newborn boy.

A genetic duplication on chromosome 5 was linked to a woman's unique combination of medical conditions.

Early diagnosis and tailored treatments are crucial for managing ichthyosis syndromes with hair abnormalities.

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

An 18-year-old man was diagnosed with a rare genetic disorder causing hair loss, severe light sensitivity, and skin issues.

Experts met to improve care for ichthyosis patients in Spain.

A girl with a rare skin condition improved after one month of treatment with acitretin.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

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

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

An 8-year-old Saudi boy was diagnosed with a rare genetic disorder causing hair loss, skin issues, and light sensitivity.

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