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Damaging mutations in NFKB2 cause a severe and distinct form of primary immunodeficiency with early-onset and often ACTH-deficiency.

A toddler with a rash and developmental delays improved after treatment for severe malnutrition caused by a diet lacking in protein.

DAVID syndrome is a condition with immune system and hormone deficiencies, needing early diagnosis to avoid serious complications.

A five-month-old boy with Omenn syndrome successfully recovered after a stem cell transplant with reduced intensity conditioning.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

The 1891 epidemic skin disease was likely caused by arsenic poisoning, possibly from beer or fish.

The guidelines suggest a detailed approach to diagnosing and treating lupus, with a focus on regular check-ups, personalized medicine, and a range of drug options for different cases.

Men generally have more severe COVID-19 cases and higher death rates than women due to biological differences.

A deficiency in the TTC7A gene causes immune problems, gut issues, and hair loss.

Nearly half of children with primary immunodeficiency disorders showed skin problems, often as the first sign of their condition.

RANK is a key target in breast cancer treatment due to its role in tumor growth and bone metastasis.

A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

Oral steroids may effectively treat recurrent intussusception in children with ILH, possibly avoiding surgery.

The document concludes that ongoing research using animal models is crucial for better understanding and treating Alopecia Areata.

Some diseases can improve the outcomes of other diseases, leading to new treatment possibilities.

Severe digestive issues in DRESS need early endoscopy for better treatment.

Certain genetic markers linked to reproductive potential were identified by their impact on a protein's ability to bind to genes.

A boy's growth and immune problems were caused by a new mutation in the STAT5B gene.

The cause of alopecia areata was unknown, and while various treatments existed, no best treatment was agreed upon.

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

Skin reactions to drugs are common and can be deadly, usually requiring stopping the drug and may be better prevented with genetic testing in the future.

The document concludes that reactivation of herpesviruses, especially HHV-6, is linked to severe symptoms and complications in drug-induced hypersensitivity syndrome.

Acne is a common skin condition linked to diet, hormones, and genetics, and early treatment can prevent scarring.

Biologics for severe asthma have known side effects, but some new risks need more study.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

Any drug can cause skin reactions, but antibiotics, NSAIDs, and psychotropic drugs are more common, with some reactions being life-threatening.

Long-COVID has diverse, long-term health impacts, especially in young people.

A Brazilian male with IFAP syndrome has a unique genetic variant causing his condition.

A one-year-old child with a genetic condition had symptoms improved by treating zinc deficiency.

A man with total hair loss also developed a rare nail condition, likely due to autoimmune issues.