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The top research priorities for congenital ichthyosis include long-term side effects of oral retinoids, best topical treatments, and treatments for itch and hair loss.

A Japanese patient with a rare genetic disorder had a less severe case than others, suggesting other factors may affect symptoms.

Men with X-linked recessive ichthyosis can still experience male-pattern baldness.

Cats and dogs with dermatophytosis show skin issues, with dogs having more severe symptoms.

The child was diagnosed with cutaneous leishmaniasis.

The rash resolved after stopping ponatinib.

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

The condition is likely inherited in an autosomal-dominant pattern.

A baby boy with 13q deletion syndrome had eye cancer, a woman's vision improved after stopping a breast cancer drug, a man developed cataracts from using Propecia, and a rare skin disorder called Lipoid Proteinosis was discussed. Also, a tool called OCT is useful for diagnosing macular diseases.

Understanding genetic mutations helps diagnose and treat skin disorders like ichthyosis.

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

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

NISCH syndrome is a rare genetic disorder affecting skin and liver, with variable symptoms and limited treatment options.

Dermatologists should recognize diverse discoid lupus signs to avoid misdiagnosis.

Dermoscopy can help diagnose oral lichen planus by identifying specific patterns.

A new gene mutation linked to a skin condition was found in a Spanish family.

A 5-year-old girl has lipoid proteinosis, causing voice issues, hair thinning, skin lesions, and tongue movement problems.

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

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

A horse with severe hair loss was diagnosed with alopecia areata and a yeast infection.

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

Epidermolytic ichthyosis can be inherited in a semidominant way with mild symptoms in carriers.

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

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

Scalp skin condition LEDS has similar features to Zoon's balanitis, a mucosal skin disorder.

A woman with lymphoma had a rare skin rash on her scalp and forehead, which was hard to diagnose but responded well to treatment.

A young man was diagnosed with trichoepitheliomas, causing thick skin and hair loss.

A rare genetic deletion in the KRT1 gene causes unique skin symptoms in a family.

An elderly woman with cancer improved after treatment for a rare skin condition with coiled hairs.

Using animal names for skin conditions helps with learning and memory.