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A rare skin condition in a 17-year-old was diagnosed late, stressing the need for careful evaluation and genetic testing.

Patients with metabolic syndrome had lower Gleason scores when diagnosed with prostate cancer.

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

A 2-year-old boy with a rare brain malformation may have Gomez–López-Hernández syndrome.

Loose Anagen Syndrome causes easy-to-pull, thin hair, mainly in young girls, and improves with age.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

A family showed a new condition with inherited hair loss and skin changes, possibly due to one genetic disorder.

The patient likely has Chrousos syndrome, a rare condition causing insensitivity to glucocorticoids, requiring high-dose dexamethasone treatment.

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

Female hair loss linked to metabolic syndrome, not in males.

Hair loss linked to higher heart disease risk in both men and women.

Androgenetic alopecia is a common hair thinning condition linked to genetics and hormones.

A new mutation in the FLCN gene linked to Birt-Hogg-Dube syndrome was found, suggesting people with certain lung collapse should be tested for this mutation and screened for kidney and colon cancer.

A 36-year-old person with a female appearance but male chromosomes was diagnosed with a rare enzyme deficiency affecting sexual development.

People with early hair loss may have higher insulin levels and a greater chance of developing metabolic syndrome.

The study concludes that Loose Anagen Hair Syndrome is a benign condition that usually improves with age but can be hard to diagnose and stressful for the family.

Satoyoshi syndrome is likely an autoimmune disease that mainly affects young women and improves with immune-related treatments.

People with androgenetic alopecia (hair loss) may have a higher risk of developing metabolic syndrome.

A 13-year-old boy with a rare genetic condition survived a heart attack and improved with treatment.

People with more than 11 skin tags, especially on the thigh, neck, or armpit, may have a higher chance of metabolic syndrome.

Thorough evaluations and conservative management can lead to positive outcomes in pediatric adrenocortical carcinoma.

Young males with severe early-onset hair loss may have a higher risk of metabolic syndrome.

Sox13 is a marker for early hair follicle development but not essential for skin and hair growth.

Accurate diagnosis of granular parakeratosis is crucial for effective treatment and improvement.

Early diagnosis and a multidisciplinary approach are key to managing Sjogren's Disease symptoms.

A child with skin and heart issues had rare genetic mutations affecting skin and heart cell cohesion.

Different gene mutations cause different types of ichthyosis, with some new mutations found.

Olmsted syndrome is a rare skin disorder causing thickened skin and other symptoms.

A man's rare tumor caused unusual nerve-related symptoms that improved after surgery.