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The brothers have congenital ichthyosis, and the older brother's eye issues are due to different genetic mutations.

Aδ-LTMRs have complex synapses with glycine, while Aβ-LTMRs have simpler ones.

A new gene mutation linked to Olmsted syndrome may increase cancer risk, suggesting the need for ongoing patient monitoring.

Knuckle darkening can be an early sign of vitamin B12 deficiency.

Elkonyxis, a rare nail condition, improved when patients stopped their nail-picking habits.

There is no significant link between alopecia areata and the PON1 enzyme polymorphisms studied.

A patient with a larger than usual genetic mutation had a broader range of symptoms for a muscle disease.

Interface dermatitis is the most common skin change in drug-induced hypersensitivity syndrome.

Psychosis can be an early sign of neuropsychiatric lupus, treatable with tailored medication.

Neotropical porcupines can get co-infected with poxvirus and Toxoplasma gondii.

A new mutation in the TRPS1 gene caused Trichorhinophalangeal syndrome in a 17-year-old, highlighting the need for genetic testing.

Thymoma in cats can cause hair loss without inflammation.

COVID-19 affects many body systems, causing a wide range of symptoms and complications.

Dynamic, light touch is sensed through a common mechanism involving Piezo2 channels in sensory axons.

Blocking GABA(A) receptors increases neuron sensitivity, showing GABA and glycine have different roles in pain.

Common gene patterns may cause skin autoimmune diseases.

People with Myotonic Dystrophy type 1 are more likely to have certain skin conditions, but not more likely to get skin cancer.

A Doberman Pinscher had a rare form of autoimmune disease causing hair loss and other severe symptoms.

A woman had a rare skin condition with recurring painful nodules that heal in 6 weeks, often without needing treatment.

PNH can occur in patients with SLE, so doctors should be aware of this.

Monilethrix causes brittle hair and hair loss, and it runs in families.

A new severe form of monilethrix syndrome includes hair loss, scalp itching, cataracts, and distinct facial features.

Mechanoreceptors convert physical touch into electrical signals through specialized nerve structures.

CD18-deficient mice developed psoriasis-like skin disease, useful for studying inflammatory skin disorders.

A 7-year-old girl was diagnosed with Netherton's Syndrome, shown by skin and hair symptoms.

ECCL should be considered in patients with specific skin and eye lesions.

Long COVID causes a wide range of long-lasting symptoms that change over time and are hard to diagnose and treat.

No systemic causes were found for the patients' conditions.

Dermatopathia pigmentosa reticularis causes skin discoloration, hair loss, and nail problems.

A woman with CHILD syndrome showed skin abnormalities, and the report suggests CHILD nevus and NEVIL might be the same condition, highlighting the need for diagnosis for genetic advice.