Search

everythinglearnresearchcommunity

for

Search:↓

Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

Doctors often diagnose Cushing's syndrome late, which worsens symptoms; earlier detection is needed.

A medication called sodium valproate likely caused a girl's hair to become kinky and dry.

Dupilumab can improve both atopic dermatitis and alopecia universalis.

A 13-year-old girl was diagnosed with juvenile lupus, showing only hair loss as a symptom.

The 'Swiss cheese' pattern in scalp biopsies can indicate trichotillomania, not just alopecia areata.

Trichothiodystrophy is a condition with brittle hair and various physical and mental issues due to low sulfur in proteins.

Five Weimaraners had a milder form of color dilution alopecia causing hair loss and skin issues.

Graham-Little syndrome causes scarring hair loss and skin bumps.

Consider Werner syndrome in young patients with early aging signs and metabolic issues.

Finasteride may cause changes in dopamine-related genes, possibly leading to post-finasteride syndrome.

WNT10A gene mutations cause short anagen hair syndrome.

Woman has discoid lupus, frontal fibrosing, and androgenetic alopecia.

Thymoma-associated multiorgan autoimmunity can cause liver damage and affects multiple organs, with limited treatment options and a generally poor prognosis.

A potential link exists between unexplained hormone deficiency, hair loss, and testicular tumors, suggesting thorough screening is needed.

Two siblings have a rare genetic condition causing curly, coarse hair.

The LMNA mutation affects skin structure even in asymptomatic carriers.

A 24-year-old man developed both alopecia areata universalis and type 1 diabetes at the same time, which is rare.

A 5-year-old girl with McCune-Albright syndrome grew abnormal hair due to the drug tamoxifen.

Temporal triangular alopecia may be linked to sebaceous nevus and shows a new pinkish background feature.

Specific brain and bone imaging findings can help diagnose Trichothiodystrophy.

Growth hormone therapy can improve growth in Netherton syndrome patients with growth hormone deficiency.

The text talks about a rare skin condition causing hair loss and suggests that people with this should also check their lung and heart health.

A medication for skin rash also unexpectedly treated hair loss in a patient.

FOXN1 duplication can cause excessive hair growth.

A new gene mutation causes vitamin D-resistant rickets and hair loss in two siblings.

A patient with Cronkhite-Canada Syndrome developed colon cancer that spread to the liver, showing the need for regular cancer checks in such patients.

A child has a rare hair and skin disorder due to specific gene variants, suggesting broader genetic testing is needed.

The condition is likely inherited in an autosomal-dominant pattern.

Loose anagen hair syndrome is caused by structural abnormalities in the hair follicle's inner root sheath.