Search

everythinglearnresearchcommunity

for

Search:↓

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.

Endoscopic forehead and brow lifting safely and consistently improves aged eyebrows, but may have complications.

A new MBTPS2 gene variant disrupts fat metabolism and collagen production, causing Osteogenesis imperfecta.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

A girl with Becker's nevus syndrome showed good improvement in breast development using spironolactone.

Transcranial electrical stimulation with bisphosphonates helps maintain bone collagen better than bisphosphonates alone.

Inverted follicular keratosis on the eyelid can be cured with surgery and has a great prognosis.

A patient with a severe scalp burn developed chronic bone infection, treated with surgery and muscle-skin flap from the back.

A 4-year-old girl had a rare hair disorder affecting only part of her scalp.

FFA is more common in postmenopausal women, can affect younger women, and may stabilize over time.

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

A rare skin condition in a boy is likely due to a specific genetic mutation pattern.

Avoiding friction and using topical treatments can significantly improve rough skin caused by repeated rubbing.

A minimally invasive brow lift can effectively manage heavy brows for a natural look.

New RIPK4 gene mutations were found to cause a type of skin and limb birth defect.

Frizzy hair is fragile and can lead to hair loss and damage if not properly cared for.

Using titanium mesh and thigh tissue is effective for complex scalp reconstruction.

Accurate diagnosis of progressive supranuclear palsy requires thorough neurological assessments and MRI.

A family was found with both Trichorhinophalangeal syndrome and Loose Anagen Syndrome, suggesting a genetic connection.

A new syndrome may link skin, growth, mental, and hair issues.

Ossification in trichilemmal cysts is more common than previously believed.

PCOS may be linked to spina bifida in young females.

A newborn girl has a rare skin condition with two ulcers on her buttock that are healing on their own.

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

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

An 8-year-old boy with bed-wetting issues suffered a severe penile injury from tying a thread around his penis, requiring urgent medical treatment to avoid worse outcomes.

Hair casts can be treated with physical removal and special shampoos.

Two patients treated with TAC for mouth fibrosis improved but developed Cushing's Syndrome symptoms.

KFSD is a rare condition causing scarring hair loss, with no effective treatment known at the time of the report.