User Posts: Dr. Huma Q. Rana, MD - Clinical Genetics, Genomics, Cytogenetics, Biochemical Genetics Specialist
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Concentric Sclerosis
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Concentric sclerosis is a rare disease where the body’s immune system attacks the white matter (myelin) in the brain in a very special pattern—alternating ...

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Concentric Demyelination
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Concentric demyelination means myelin (the insulation around nerve fibers) is lost in round, ring-like layers. On MRI and under the microscope, you see ...

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Balo Concentric Sclerosis (BCS)
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Baló concentric sclerosis (BCS) is a very rare demyelinating disease. “Demyelinating” means the immune system strips the protective myelin coating from nerve ...

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Baller–Gerold Syndrome (BGS)
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Baller–Gerold syndrome (BGS) is a very rare genetic condition in which some skull bones fuse too early (craniosynostosis) and the bones on the thumb-side of ...

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Ciliary Dysentery Caused by Balantidium Coli
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Ciliary dysentery is a bowel infection caused by a large, single-cell parasite named Balantidium coli. It is the only ciliated protozoan known to infect ...

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Balantidial Dysentery
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Balantidial dysentery is a bowel infection caused by a single-celled parasite called Balantidium coli (also written in newer papers as Balantioides coli; older ...

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Balantidiasis
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Balantidiasis is an infection of the large intestine caused by a single-celled parasite called Balantidium coli (also known in newer science papers as ...

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Malignant Hyperthermia Syndrome
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Malignant Hyperthermia Syndrome is a dangerous reaction of the body’s skeletal muscles to some anesthesia medicines. In people who carry certain inherited ...

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Congenital Myopathy–Cleft Palate–Malignant Hyperthermia Syndrome
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Congenital Myopathy–Cleft Palate–Malignant Hyperthermia Syndrome is a rare, inherited muscle disease starts at birth (congenital). Babies have weak muscles (a ...

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Congenital Myopathy 13 (CMYP13)
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Congenital myopathy 13 is a rare, inherited muscle condition that starts at birth. It is caused by changes (variants) in a single gene called STAC3. This gene ...

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Bailey-Bloch Congenital Myopathy (STAC3 Disorder)
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Bailey-Bloch congenital myopathy is a rare, inherited muscle disease that starts at birth. It mainly affects skeletal muscles (the muscles we use to move). ...

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Bagatelle–Cassidy Syndrome
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Bagatelle–Cassidy syndrome is an extremely rare condition first described in a single child in the medical literature. The main pattern includes a large head ...

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Bacterial Infectious Meningitis
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Bacterial infectious meningitis is a rapidly dangerous illness where bacteria infect the meninges — the thin protective layers that cover the brain and spinal ...

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Baby Rattle Pelvis Dysplasia
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Baby Rattle Pelvis Dysplasia is a very rare, severe skeletal disorder seen before birth or at birth. It was first described in the medical literature as a new, ...

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Piroplasmosis
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Piroplasmosis, also called babesiosis, is an infection caused by tiny parasites that live inside red blood cells. These parasites are usually from the Babesia ...

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Babesiosis
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Babesiosis is a disease caused by tiny parasites (called Babesia) that live inside red blood cells. These parasites are carried by black-legged ticks (also ...

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Congenital Disorder of Glycosylation Type IId (B4GALT1-CDG)
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Congenital disorder of glycosylation type 2d (CDG-IId) is an ultra-rare, inherited, multi-system metabolic disease caused by damaging variants in the B4GALT1 ...

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Carbohydrate-Deficient Glycoprotein Syndrome Type 2d (CDG-IId)
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Carbohydrate-Deficient Glycoprotein Syndrome Type 2d (CDG-IId) is a very rare inherited disease that affects how the body builds sugar chains (glycans) on ...

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Beta-1,4-Galactosyltransferase Deficiency (B4GALT1-CDG)
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Beta-1,4-galactosyltransferase deficiency is a very rare, inherited metabolic disease. It belongs to a family of conditions called congenital disorders of ...

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B4GALT1-CDG (Beta-1,4- Galactosyltransferase 1 Deficiency)
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B4GALT1-CDGB4GALT1-CDG (Beta-1,4- Galactosyltransferase 1 Deficiency) is a very rare inherited condition in which the body cannot correctly attach certain ...

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B4GALT1-Congenital Disorder of Glycosylation (B4GALT1-CDG)
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B4GALT1-Congenital Disorder of Glycosylation (B4GALT1-CDG) is a very rare inherited condition that changes the way the body adds sugar chains to proteins (a ...

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B-Cell Prolymphocytic Leukemia (B-PLL)
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B-cell prolymphocytic leukemia is a rare, aggressive leukemia that arises from mature B-lymphocytes (a type of white blood cell). Under the microscope, the ...

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B-cell Prolymphocytic Leukemia (B-PLL)
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B-cell prolymphocytic leukemia is a very rare, fast-growing cancer of mature B-lymphocytes (a type of white blood cell). In this disease, the blood, bone ...

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Grey Zone Lymphoma
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Grey zone lymphoma (now called mediastinal grey zone lymphoma, MGZL, in the 5th edition WHO classification) is a rare cancer of B-lymphocytes that shows ...

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B-cell Lymphoma, Unclassifiable, with Features Intermediate Diffuse Large B-cell Lymphoma
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B-cell Lymphoma, Unclassifiable, with Features Intermediate Diffuse Large B-cell Lymphoma  are cancers that begin in B-cells, a type of white blood cell that ...

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B-Cell Lymphocytic Neoplasms
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B-cell lymphocytic neoplasms are cancers that begin in B-cells, a type of white blood cell that makes antibodies. These cancers grow in the lymph nodes, bone ...

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What is B – Cell Lymphoma?
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B-cell lymphoma is a cancer that starts in B lymphocytes, which are white blood cells that normally make antibodies to help you fight germs. In lymphoma, some ...

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Chronic Lymphoplasmacytic Leukemia (CLLPL/LPL)
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Chronic lymphoplasmacytic leukemia (often called Waldenström macroglobulinemia) is a slow-growing cancer of B-cells that behave like a mix of small lymphocytes ...

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B-Hematopoietic Chronic Lymphocytic Leukemia (CLL)
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B-Hematopoietic Chronic Lymphocytic Leukemia (CLL) is a slow-growing blood cancer. It starts from B lymphocytes—a kind of white blood cell that is made in the ...

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B-Familial Chronic Lymphocytic Leukemia (B-CLL)
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B-familial chronic lymphocytic leukemia is a slow-growing blood cancer that starts in B lymphocytes (a type of white blood cell that helps make antibodies). In ...

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Chronic Lymphatic Leukemia
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Chronic lymphocytic leukemia (CLL) is a slow-growing blood cancer. It starts when a group of white blood cells called B-lymphocytes in the bone marrow begin to ...

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B-cell Chronic Lymphocytic Leukaemia (CLL)
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B-cell chronic lymphocytic leukaemia (CLL) is a slow-growing cancer of the blood and bone marrow. It starts from B lymphocytes (B cells), a type of white blood ...

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B-Cell Chronic Lymphogenous Leukaemia (CLL)
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B-cell chronic lymphogenous leukaemia is a slow-growing blood cancer that starts in B lymphocytes, which are white blood cells that help your immune system ...

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B-Cell Chronic Lymphocytic Leukemia (CLL) / Small Lymphocytic Lymphoma (SLL)
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B-cell chronic lymphocytic leukemia (CLL) / small lymphocytic lymphoma (SLL) is a blood and bone-marrow cancer. It starts from B lymphocytes (a type of white ...

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B-Cell Chronic Lymphocytic Leukemia (CLL)
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B-Cell Chronic Lymphocytic Leukemia (CLL) is a slow-growing blood cancer where the bone marrow and lymph nodes produce too many abnormal B-lymphocytes. These ...

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