Search

everythinglearnresearchcommunity

for

Search:↓

People with hypohidrotic ectodermal dysplasia are more likely to experience long-term fatigue and hair loss after COVID-19.

Hair loss in Cronkhite-Canada syndrome may be caused by autoimmune factors, not just stress or malabsorption.

A 16-year-old girl with autoimmune hemolytic anemia and deep vein thrombosis improved with treatment, possibly indicating systemic lupus erythematosus.

Higher DKK-1 levels found in hair loss patients; L-ascorbic acid 2-phosphate, L-threonate, and ginsenoside F2 may help promote hair growth.

Kainar syndrome symptoms may be linked to nuclear test exposure effects.

Proper diet management is crucial for phenylketonuria patients to avoid severe health issues.

A 7-year-old girl was diagnosed with trichothiodystrophy due to low sulfur levels in her hair.

Early phosphorus-calcium disorders in children with chronic kidney disease can lead to bone issues, highlighting the need for early bone density testing.

Inherited ichthyoses cause widespread skin scaling and thickening due to gene mutations.

Two enzyme defects in biotin metabolism cause severe skin, hair, and metabolic issues.

New mutations in hair keratin genes can change hair structure and cause monilethrix, with nail issues more common in certain gene mutations.

Vitiligo often starts young, is linked to family history and stress, and requires comprehensive care including psychological support.

Vitamin D receptor is essential for healthy bones and skin.

Ayurvedic treatment reduced hair loss and improved scalp health effectively.

CD8+ virtual memory T cells may cause hair loss in alopecia areata.

A new IL6ST gene variant may cause a unique form of hyper-IgE syndrome with skin abscesses and high IgE levels.

COVID-19 vaccination may trigger recurrence of cutaneous T-cell lymphoma in some patients.

The meeting showcased rare skin disease cases, highlighting the need for accurate diagnosis and treatment.

A unique gene mutation was found in a family with monilethrix.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

A woman lost all her body hair after hepatitis C treatment, but it started to grow back a year after stopping the treatment.

A girl with hereditary chorea, likely Huntington's disease, had her condition worsened by lupus.

Dermatologists should be involved in the care of hematology patients due to common skin issues.

Too much vitamin A can cause serious health problems.

CARASIL, a rare genetic disorder, was confirmed in an Arabic woman, highlighting its rarity and need for stroke prevention.

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

The LMNA mutation affects skin structure even in asymptomatic carriers.

RHUPUS should be considered in children with deforming arthritis.

THA is a rare condition with no significant clinical consequences if thyroid function is normal.

A child with eruptive vellus hair cysts showed some improvement with calcipotriene cream.