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Combining traditional Chinese medicine with microneedles shows promise for effectively treating skin diseases with fewer side effects.

Bird-related analogies help explain and remember skin conditions better.

Creatine monohydrate is safe and effective for muscle recovery and performance, especially for those with low creatine levels.

Testosterone with finasteride improved muscle and bone health in men with spinal cord injury.

The new hair transplant device reduces damage to hair follicles and makes surgery more comfortable for the surgeon.

Gender-affirming hormone therapy improves physical performance in trans men to the level of cisgender men, while in trans women, it increases fat mass and decreases muscle mass, with no advantage in physical performance after 2 years.

Spinal fMRI can help understand brainstem and spinal cord function, especially in spinal cord injury patients.

A 3D model of Dupuytren’s disease was developed for better drug testing.

Trichothiodystrophy causes unusual hair and developmental issues.

MCTD should be considered in children with recurring muscle issues, lupus-like symptoms, and edema.

The neck mass was a rare benign "wattle," surgically removed for diagnosis and appearance.

Danon disease can be hard to diagnose due to non-specific symptoms.

A man with myotonic dystrophy type 1 had 28 skin cancers, suggesting a link between the disease and skin cancer, emphasizing the need for sun protection and regular skin checks.

The newborn was diagnosed with a rare skin disorder causing blisters, which requires careful wound care and family support.

Penile strangulation from hair can cause severe harm but can be treated if caught early.

Finasteride significantly reduced tics and obsessive-compulsive symptoms in Tourette syndrome patients.

Inverted Follicular Keratosis is rare but should be considered in scalp lesion diagnoses for all ages.

A girl with a rare syndrome had successful hair loss treatment with no relapse after 4 years.

Griseofulvin effectively treats tinea capitis in infants.

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

Olmsted syndrome can be inherited as an autosomal recessive trait due to a rare TRPV3 gene mutation.

The pseudo 'fringe sign' can also appear in frontal fibrosing alopecia, not just in traction alopecia, showing that this condition may be more common than thought.

Undiagnosed lupus can cause severe complications after epidural anesthesia, leading to muscle weakness and potentially death.

Rothmund-Thomson syndrome causes skin changes, hair loss, and slightly high lysine and cystine in urine.

A boy with monilethrix has brittle hair that breaks easily due to a genetic condition, which might improve by puberty.

A girl's severely tangled hair couldn't be fixed and had to be cut due to a rare condition called plica neuropathica.

Capsaicin cream quickly relieved itching in two patients with brachioradial pruritus.

A woman with undifferentiated connective tissue disease was diagnosed with renal amyloidosis and carpal tunnel syndrome.

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