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Bullous pemphigoid, intrahepatic cholangiocarcinoma, and alopecia areata may share immune-related causes.

Two Australian Poll Hereford calves had severe anaemia, abnormal red blood cells, and skin issues.

Patients with both connective tissue disease and acid reflux are more likely to have certain symptoms and physical signs.

Early recognition and a team approach are crucial for managing diffuse alveolar hemorrhage in antiphospholipid syndrome.

Certain mouse strains develop a skin condition similar to a human hair loss disease due to genetic defects.

The curly mutation in SELH/Bc mice affects hair and may help study human genetic disorders.

A 20-year-old woman with a rare form of Turner syndrome showed improvement with hormonal therapy and needs comprehensive care.

Hair-Thread Tourniquet Syndrome is a rare condition where hair or thread tightly wraps around a child's body part, requiring quick treatment to prevent damage.

The keratin 5 mutation in a family with epidermolysis bullosa simplex was due to mosaicism, not a new mutation.

Early diagnosis and genetic counseling are crucial for managing adrenoleukodystrophy.

Early recognition and management of gastrointestinal tuberculosis in lupus patients are crucial to prevent complications.

Biotinidase deficiency can cause symptoms like sleepiness, hair loss, and seizures.

Tick bites can cause hair loss similar to alopecia areata, and baricitinib may help regrow hair.

BBS7 is crucial for maintaining healthy periodontal ligaments by supporting Shh signaling.

A woman was wrongly diagnosed with lupus but actually had leprosy.

A 33-year-old woman with PCOS and metabolic syndrome was unusually diagnosed with a bone condition called DISH, suggesting a possible link between these conditions.

A 4-year-old girl has a rare condition causing hairlessness and skin bumps, but normal teeth and sweating.

A woman with a rare hormone resistance condition also had missing teeth and hair loss, which might be new symptoms of her genetic disorder.

Middle Eastern patients with epidermolysis bullosa show specific genetic mutations linked to different types of the disease.

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.

A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

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

Localized dystrophic epidermolysis bullosa (DEB) can lead to scarring alopecia, highlighting the need to recognize and address this complication.

A man with hypoparathyroidism had other health issues that led to a diagnosis of a rare autoimmune disorder, APS-1.

A calf in Scotland likely had Schmallenberg virus from its mother.

Research on Hutchinson-Gilford progeria syndrome could help understand normal aging and heart disease.

High androgen levels and genetic factors likely cause Becker's nevus and related symptoms.

Baricitinib reduces inflammation and improves cell health in premature aging cells.

A patient with a rare chromosome condition also had a rare type of hair loss.