Search

everythinglearnresearchcommunity

for

Search:↓

A Doberman Pinscher had a rare form of autoimmune disease causing hair loss and other severe symptoms.

Skin cells might help spread prion diseases like Creutzfeldt-Jakob disease.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

The KRTAP21-2 gene affects wool length and quality in sheep.

The study concludes that early diagnosis of Frontal Fibrosing Alopecia is important, as it is often found in postmenopausal women, may be related to Lichen Planopilaris, and eyebrow hair loss is a common sign.

Applying InlB321/15 to wounds sped up healing in mice.

Different versions of the KRTAP6-2 gene in goats can lead to thinner cashmere fibers.

Most women with polycystic ovary syndrome (PCOS) have menstrual issues, infertility, acne, and excessive body hair, with the most common type being the non-androgenic phenotype.

Mutations in specific llama genes may affect fiber quality for textiles.

The document concludes that specific hair and blood vessel abnormalities in infants with seizures and developmental issues may indicate Menkes disease, which lacks a cure and is often fatal by age 3.

Oral lichen planus can appear before lichen planopilaris.

Genomic profiling for myeloid cancers can find important inherited mutations, but it's challenging when these mutations aren't related to the patient's symptoms.

A patient with Wilson's disease showed hair-pulling behavior as an initial symptom.

A 36-year-old person with a female appearance but male chromosomes was diagnosed with a rare enzyme deficiency affecting sexual development.

A man with Isaac's syndrome affecting only one side of his body improved after immune system-targeted treatment.

New hair loss subtype found, mimics common baldness.

Frontal Fibrosing Alopecia is a slowly progressing hair loss condition, likely underdiagnosed, with ineffective treatments, needing more research to understand it fully.

Genetic variants can affect valproic acid's effectiveness, side effects, and levels in epilepsy treatment.

Ayme-Gripp Syndrome was confirmed in a woman through genetic testing, highlighting the need to consider rare genetic conditions in diagnoses.

The woman has a rare skin condition called follicular Dowling-Degos disease, which has limited treatment options.

High CRP levels could indicate vitamin D deficiency in people with alopecia areata.

Cryptococcoid Sweet syndrome can be linked to hydralazine use and multiple autoantibodies, requiring high clinical suspicion and more research.

A child with a rare vitamin D-resistant condition improved with treatment.

A 61-year-old Filipino man had a skin condition that looked like another disease, making diagnosis difficult.

Most women with long-term, widespread hair loss need a tissue examination for an accurate diagnosis.

Boron deficiency in maize affects leaf boron levels and nutrient uptake differently depending on root hair presence and soil type.

The KRTAP36-2 gene in sheep affects wool yield.

Using both minoxidil and finasteride together on the scalp works better for male hair loss than using either one alone.

The most common form of PCOS in the group was anovulatory PCOS, with no cases of obese PCOS, highlighting the importance of assessing lean women with menstrual issues.

A patient with a new PLEC gene mutation showed symptoms of both muscular dystrophy and myasthenia gravis, which improved with steroid treatment.