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Genetically at-risk healthy people show similar immune issues as those with Pemphigus vulgaris or Alopecia areata.

Mutations in the TSPEAR gene cause a new form of ectodermal dysplasia affecting hair and tooth development.

A 6-year-old girl was diagnosed with a rare hair disorder called monilethrix.

Plica neuropathica can be a sign of schizophrenia and improves with antipsychotic treatment.

Reducing immunosuppression and using antiviral creams improved the woman's skin condition.

Genetic hair shaft abnormalities can be seen with microscopes and often affect scalp hair.

EPDS can cause recurring scalp sores and hair loss if not treated.

Cicatricial pattern hair loss is likely advanced common baldness, not a type of lichen planopilaris.

Zinc supplements and genetic analysis help treat acrodermatitis enteropathica in children.

A 10-year-old boy's nail condition is mainly cosmetic and improves over time with treatment.

The man's hair loss and skin papules were diagnosed as atrichia with papular lesions, not alopecia areata universalis.

Histone modification is key in treating chronic inflammatory skin diseases.

Alopecia can be caused by multicentric reticulohistiocytosis.

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

Children with different rheumatologic diseases have specific skin symptoms that can help with diagnosis.

Friedreich's ataxia causes thin, weak hair with surface damage and cavities.

The skin issues in the two dogs might be caused by infection or self-injury, not genetics.

The protein called small nuclear ribonucleoprotein polypeptide E is identified as a cause of a type of hair loss without other symptoms.

Dermoscopic and histopathological features combined can help diagnose Pityriasis versicolor.

Trichorrhexis invaginata can occur with tinea capitis, though it's rare.

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

A Persian cat had a rare skin condition that didn't improve with treatment.

Scalp pemphigus vulgaris can be effectively treated with low-dose prednisone and triamcinolone.

Mutations in hKAP1 genes may cause hereditary hair disorders.

Deep phenotyping helps distinguish between xeroderma pigmentosum and trichothiodystrophy, aiding in diagnosis and treatment.

Koilonychia in alopecia areata can improve with oral corticosteroids.

A girl inherited excessive body hair from her mother and grandmother.

Melanoma risk tools need improvement, a gene mutation causes a hair disorder that might be treated by managing cell stress, a potential therapy for a skin-ear disorder involves blocking cell channels, skin wrinkling may indicate lung aging regardless of smoking, and oxidative stress might contribute to common baldness.

A chimeric keratin partially improved skin structure in mice lacking keratin 5, but didn't fully restore normal skin.