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Erosive palmoplantar lichen planus in North-East India mainly affects the feet and often involves nails, with unique inflammatory skin changes.

A 70-year-old woman with bronchiectasis developed a rare immune disease due to a bacterial infection, requiring a difficult balance of treatments.

Patients with certain FoxN1 gene mutations have severe immune issues but normal skin and hair.

Netherton syndrome causes specific skin and hair changes that help in early diagnosis.

An elderly woman's swollen, painful foot was found to be caused by a rare type of bone lymphoma, which improved with radiation treatment.

Genetically repaired stem cells may treat certain genetic diseases, Th17 cells are key in fighting systemic fungal infections, hair loss in AGA is due to progenitor cell loss, and α-synuclein transfer might contribute to Parkinson's disease progression.

A specific gene mutation causes Olmsted syndrome.

Glycine is a key transmitter in rat spinal cord synapses, often alongside GABA.

Psoriasis or contact dermatitis can override alopecia areata, allowing hair growth.

Skin lesions in Carney complex are likely caused by a specific group of skin cells that promote pigment production due to a genetic mutation.

Biotin treatment improves symptoms of biotinidase deficiency, but some neurological damage may be permanent.

Exosomes from stem cells help improve nerve repair in rats.

Neuropilin 2 may be a biomarker for melanoma and affects melanocyte behavior.

New insights into cell communication in psoriasis suggest innovative drug treatments.

A person with a specific gene mutation had extra teeth, unique jaw and hair features not seen before in this condition.

Microneedle arrays deliver botulinum toxin effectively for sweat suppression, similar to injections.

Nanofiber scaffolds show promise for improving nerve healing.

New mutations in hair keratin genes can change hair structure and cause monilethrix, with nail issues more common in certain gene mutations.

H1 increases risk for neurodegenerative diseases, while H2 offers protection but is linked to other disorders.

Procyanidins from grape seeds reduce nerve pain by blocking specific proteins and inflammation.

Carriers of a specific gene mutation have subtle skin changes without visible symptoms.

Carbamazepine may cause lung problems and lupus-like symptoms, which can improve after stopping the drug.

Necrobiosis lipoidica may need new criteria for accurate diagnosis due to similarities with another condition.

A hereditary condition causes hair loss and twisted hair in some family members.

Toxic Epidermal Necrolysis is a rare, serious skin condition that can affect anyone, is more common in women, and may be linked to genetics, with a 20% mortality rate mainly due to sepsis.

A rare skin disorder, nevus comedonicus, can appear on one side of the body following Blaschko's lines.

Resident memory T cells and necroptosis may drive fibrosis in eosinophilic fasciitis and morphea.

Mixed Connective Tissue Disease can develop from overlapping symptoms of several autoimmune diseases, making diagnosis complex.

TRPA1 is crucial for mechanical sensitivity in skin sensory neurons.