Rx Autoimmune, Genetic and Rare Diseases (A – Z)
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Acute Necrotizing Hemorrhagic Leukoencephalitis (ANHL)
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Acute necrotizing hemorrhagic leukoencephalitis (ANHL) is a very rare, sudden, and severe inflammation of the brain’s white matter. Doctors also call it “Hurst ...

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Acute Hemorrhagic Leukoencephalitis (AHLE)
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Acute hemorrhagic leukoencephalitis (AHLE) is a very rare, very fast-moving disease of the brain. It is a severe form of inflammation that attacks the white ...

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Fulminant Graft-Versus-Host Disease (GVHD)
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Fulminant GVHD is a sudden, very severe form of acute GVHD that happens after a stem-cell or bone-marrow transplant. In GVHD, donor immune cells (mostly ...

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Acute Graft-versus-Host Disease (aGVHD)
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Acute graft-versus-host disease (aGVHD) is a complication after an allogeneic hematopoietic stem-cell or bone-marrow transplant. Donor immune cells (mainly T ...

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Acute Myeloid Leukaemia M6
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Acute myeloid leukaemia M6 is an aggressive blood cancer where very early red-blood-cell precursors (erythroblasts) grow out of control in the bone marrow. ...

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Acute Erythroblastic Leukaemia
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Acute erythroblastic leukaemia is a very rare and aggressive blood cancer. It starts in the bone marrow, where red blood cells are made. In this disease, very ...

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Acute Kernicterus
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Acute kernicterus—better called acute bilirubin encephalopathy (ABE)—is a type of brain injury that happens in newborns when unconjugated (indirect) bilirubin ...

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Acute Bilirubin Encephalopathy
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Acute bilirubin encephalopathy (ABE) is brain injury in a newborn caused by very high levels of unconjugated (indirect) bilirubin. When bilirubin gets too ...

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Senescent T-cells–Lymphadenopathy–Immunodeficiency Syndrome
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This condition is a rare, inherited immune system disorder in which a signaling switch inside white blood cells (the PI3K-delta pathway) is stuck “too on.” ...

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Activated PI3K-Delta Syndrome (APDS)
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Activated PI3K-delta Syndrome (APDS) is a rare, inherited immune system condition. It happens when a key signaling pathway in white blood cells (called the ...

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Progressive Myoclonic Epilepsy (PME)
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Progressive Myoclonic Epilepsy (PME) is a group of rare genetic epilepsy disorders. They cause myoclonus (sudden jerks), seizures, and over time problems with ...

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Myoclonus Nephropathy Syndrome
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Myoclonus-nephropathy syndrome is a rare genetic disorder in which two problems happen together and often get worse over time. The first problem is a ...

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Action Myoclonus–Renal Failure (AMRF) Syndrome
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AMRF is a very rare inherited disease. It has two big parts that often progress independently: a progressive myoclonic epilepsy (sudden jerks that are ...

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Madura Foot Due to Actinomadura (Actinomycetoma of the Foot)
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Madura foot” is a slow, chronic infection of the foot that starts after tiny breaks in the skin let soil-living germs enter. When the germ is a ...

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Actinomycotic Mycetoma of Foot
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Actinomycotic mycetoma of the foot—often shortened to actinomycetoma—is a chronic, slowly progressive infection of the skin, subcutaneous tissue, and sometimes ...

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Actinomycotic Madura Foot (Actinomycetoma)
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Actinomycotic Madura foot is a slow, long-lasting infection of the skin and deeper tissues of the foot caused by special bacteria called actinomycetes (for ...

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Actinomycosis
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Actinomycosis is a long-lasting bacterial infection. It is caused by Actinomyces bacteria. These bacteria normally live harmlessly in the mouth, throat, gut, ...

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Summertime Actinic Lichenoid Eruption (SALE)
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Summertime actinic lichenoid eruption (SALE) is a sun-induced, seasonal skin disorder. It is part of the lichenoid family of rashes, which means the top layer ...

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Lichenoid Melanodermatitis
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Lichenoid melanodermatitis is an older umbrella label dermatologists used for sun-exposed or photo-accentuated, dark-brown to grey patches and plaques that ...

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Acrorenal Syndrome
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Acrorenal syndrome is a rare condition present at birth. It affects the growth of the hands and feet (“acro”) and the kidneys and urinary tract (“renal”). The ...

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