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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.

Low SHBG levels are linked to negative health outcomes and should be used in assessing and managing health conditions.

Sonic hedgehog (Shh) is crucial for gecko tail regeneration.

Doctors often miss Hair Tourniquet Syndrome, which can lead to serious damage if not treated quickly.

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.

A 12-year-old boy had severe shingles and skin damage after a stem-cell transplant.

New findings suggest the protein linked to Birt–Hogg–Dubé syndrome is important in cell signaling and could affect treatment understanding.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

A rare hair follicle disorder can cause itchy, bluish-black bumps on the body.

SHPro® improved urinary symptoms and erectile function in men and is safe.

The 3D-SeboSkin model effectively simulates Hidradenitis suppurativa and is useful for future research.

Beta-trace protein may help diagnose and predict treatment response in certain nerve disorders.

Trichostatin A helps restore hair-growing ability in skin cells used for hair regeneration.

A baby boy's toe was saved from damage caused by hair strangulation by quick surgical treatment.

27 out of 32 candidates passed the hair restoration surgery exam.

A child with trichothiodystrophy also had autoimmune thyroiditis and anemia, which is a new finding.

Hutchinson-Gilford Progeria Syndrome caused rapid aging due to a genetic mutation, with treatments to manage symptoms.

Trichothiodystrophy causes unusual hair and developmental issues.

Gender affirming hormone therapy improves outcomes in gender affirmation surgery.

Permanent hair removal with lasers may cure itchy black hair bristles on the back.

Gender-affirming hormone therapy improves mental health and gender incongruence but requires careful management of cardiovascular and cancer risks.

A new mouse mutation causes skin and hair defects due to a gene change.

Dermoscopy can help diagnose tuberous sclerosis by identifying unique skin patterns.

BST2 is a key marker for hair loss disease alopecia areata.

RNA-based treatments show promise for managing Hutchinson-Gilford Progeria Syndrome.

A gene deletion in DSG4 causes sparse hair in some Pakistani families.

A rare skin condition was confirmed to be associated with a specific virus in a young girl.