Search

everythinglearnresearchcommunity

for

Search:↓

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

CTA is often mistaken for AA but doesn't respond to steroids and may require hair transplantation.

A rare finger tumor was imaged, showing a unique pattern not seen before.

A person with Turner Syndrome showed severe schizophrenia that didn't respond to treatment and had brain shrinkage.

Early recognition and treatment of VATS in transplant patients improve outcomes.

A 6-year-old girl with Turner syndrome also had psoriasis, alopecia areata, and trachyonychia.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

Rapamycin and anti-EGFR antibody reduce LAM/TSC cell migration and blood vessel growth in the uterus.

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

Multiple pilomatrixoma may indicate Turner syndrome.

A 23-year-old Syrian woman has two rare hair disorders, and avoiding hair treatments plus using vitamins and minoxidil may help.

The virus linked to a rare disease was found in a patient's blood and urine before skin symptoms appeared.

Multiple perifollicular fibromas may actually be unrecognized cases of Birt-Hogg-Dubé syndrome.

A rare benign tumor with hair follicle features was found on a man's trunk.

SV40 T antigen in hair follicles causes abnormal hair and health issues in mice.

Trichodysplasia spinulosa is a rare skin condition caused by a virus, treatable with antiviral medication.

An infant developed excessive hair growth after a bone marrow transplant and cyclosporine treatment.

Turner's syndrome may be linked to autoimmune diseases like psoriasis and alopecia areata, needing comprehensive care.

TTD hair brittleness is caused by multiple structural abnormalities.

The study found that Tourette Syndrome may be linked to certain immune system processes and synaptic signaling.

A rare scalp tumor was removed from a 49-year-old woman, with a good outlook if benign but needing careful monitoring if malignant.

A rare family case of multiple benign hair follicle tumors was identified, highlighting the need to distinguish them from similar conditions.

Consider TFI in facial hypopigmentation diagnoses and confirm with a biopsy.

Fragile hair in children is rarely linked to trichothiodystrophy (TTD).

Seborrheic keratosis is a common, harmless skin growth that can look like cancer, so it may need a biopsy.

Tay syndrome is a unique genetic disorder causing skin, hair, and developmental issues.

Mutations in the TSPEAR gene cause a new form of ectodermal dysplasia affecting hair and tooth development.

Temporal triangular alopecia in infants is mostly seen in males at birth, with unique features that help with diagnosis.

Some skin tumors from hair follicles and glands can be linked to genetic syndromes and may be benign or malignant.

Steatocystoma multiplex causes recurring skin cysts and needs early recognition for better management.