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Infants with severe KID syndrome may be more prone to serious infections and need close monitoring.

A 4-year-old girl with a rare lupus condition was successfully treated with oral corticosteroids, leading to full recovery and hair regrowth.

Finasteride negatively affects fish reproduction and gonadal development.

Fluocinolone may help treat scalp symptoms in ichthyosis patients.

Gluconolactone products can significantly reduce skin scaling in golden retrievers with ARCI.

Dermoscopy may not show hookworms clearly, and comparing it with tissue studies could improve diagnosis accuracy for skin conditions caused by parasites.

Symmetrical Acrokeratoderma (SAK) may be a unique skin condition in China, lacking specific treatment and needing long-term monitoring.

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

A rare skin condition in a baby showed unusual fat and hair follicle changes.

The cat's skin condition was resistant to treatment and did not improve.

A rare skin condition in a boy is likely due to a specific genetic mutation pattern.

Terrestrial vertebrates have balanced keratin gene clusters, unlike teleost fish.

A mutation in the SREBF1 gene causes both hereditary mucoepithelial dysplasia and IFAP syndrome, which are related conditions.

Different fish use the same genes to regrow teeth.

A boy with a rare skin condition and kidney disease improved with cyclosporine after steroids failed, suggesting a new treatment approach.

Long-read RNA sequencing can identify complex gene changes in IFAP syndrome.

Flexural follicular lichen planus is a rare skin condition affecting body folds.

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

Lymphangiosarcoma was confirmed in cats with specific skin symptoms using a lymphatic marker.

The yeast found in a sea lion's skin lesion was almost identical to that on healthy skin, suggesting environmental factors may affect fungal growth and the cause of the lesion is unclear.

Different whale and dolphin species have unique whisker follicle structures, suggesting they might use their whiskers in various ways.

Manatee whiskers are specially adapted for touch in water.

Hormonal changes during the reproductive cycle may cause seasonal skin problems in captive female fossas.

A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.

Cholesterol sulfate buildup due to a genetic mutation disrupts the skin barrier, leading to the scaling skin seen in X-linked ichthyosis.

Tay syndrome is a unique genetic disorder causing skin, hair, and developmental issues.

Zebrafish skin regeneration relies on cell behaviors and reactive oxygen species, with antioxidants reducing and hydrogen peroxide increasing regeneration.

Lichen spinulosus, usually seen in young people, can rarely occur in adults, as shown by a 52-year-old woman with a rough, bumpy rash.

The horse had a rare type of hair loss caused by immune cells attacking hair follicles.

The document reports a rare case of ECCL with a new association with optic disc colobomas.