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Rhodococcus equi causes severe pneumonia in young foals, and effective vaccines are needed due to foals' weak immune responses.

An 8-year-old girl developed a rare skin condition in a linear pattern on one side of her body after a lung infection, which improved with treatment.

A girl with Crohn's disease had a hairball causing bowel obstruction, which was removed, and she recovered well.

Tinea capitis is common in the Eastern Province of Saudi Arabia and can be effectively treated.

Eating grape powder may reduce the severity of skin allergy symptoms.

The girl had a rare disorder causing mental and physical symptoms, with weak hair and unclear neurological issues.

GnRH agonists can help manage recurrent priapism in sickle cell patients, but long-term safety is unclear.

Tinea faciale can be mistaken for lupus due to similar symptoms.

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.

Children with atopic diseases have a higher risk of developing alopecia areata.

Doctors should use a detailed patient history and physical exam to diagnose joint pain, and consult a rheumatologist early for suspected autoimmune diseases.

Timely diagnosis and aggressive treatment with high-dose steroids and B-cell depletion therapies are effective for severe acute cutaneous lupus.

Patients with alopecia areata should be checked for muscle spasms, diarrhea, and ANA to avoid missing Satoyoshi syndrome.

Tinea capitis is a scalp fungal infection in children that can cause hair loss, scaling, and other symptoms.

People with Down syndrome have higher rates of certain immune-related conditions and need special medical attention.

A mutation in the SREBF1 gene causes both hereditary mucoepithelial dysplasia and IFAP syndrome, which are related conditions.

A 6-year-old boy's skin condition improved after stopping a specific treatment and starting new medications.

An 87-year-old woman was diagnosed with type 3 autoimmune polyendocrine syndrome and had multiple autoimmune issues.

Juvenile dermatomyositis can worsen quickly and needs strong treatment.

A 21-day-old baby had a skin rash that didn't improve with cream and wasn't caused by a fungus.

Some children with methylmalonic and propionic acidaemias have skin problems related to their condition and diet.

A pregnant woman with Cushing Syndrome got worse and sadly passed away.

Graves' disease can cause hair loss in children and should be considered when treating pediatric alopecia areata.

Early diagnosis and treatment of TPP can prevent complications.

An infant with Hutchinson-Gilford Progeria Syndrome had successful surgery to fix breathing issues caused by a new genetic mutation.

The clinical signs of Adams-Oliver syndrome can vary greatly, even among family members.

A man with itchy skin lesions and weight loss was diagnosed with a rare skin condition linked to a pancreatic tumor.

Overexpression of the glucocorticoid receptor in mice causes developmental defects similar to ectodermal dysplasia.

Nirogacestat can cause severe skin issues like hidradenitis suppurativa.

Pregnant women with COVID-19 and gestational diabetes may face severe complications, and more research is needed on their outcomes.