Dr Rahul Bhargava

Treatments

Anemia

Anemia is a condition characterized 

Acute Myelogenous Leukemia

(AML) is a fast-growing cancer of

Amyloidosis

Amyloidosis is a rare and serious

Acute Lymphocytic Leukemia

(ALL), also known as Acute

Antiphospholipid Syndrome

Antiphospholipid Syndrome

(APS) is an autoimmune disorder

Benign Hematologic Conditions

Benign Hematologic Conditions

Benign hematologic conditions are

Autoimmune Thrombocytopenia

Autoimmune Thrombocytopenia

also known as Immune

Autoimmune Hemolytic Anemias

Autoimmune Hemolytic Anemias

Welcome to the specialized

Aplastic Anemia

Aplastic Anemia

Aplastic anemia is a rare and

Bleeding Disorders

Bleeding Disorders

Bleeding disorders are a group

Castleman Disease

(CD) is a rare and complex

CMML

(CMML) is a rare and serious

Chronic Lymphocytic Leukemia

(CLL) is a type of cancer that

Chronic Myelogenous Leukemia

(CML) is a type of cancer that

Cryoglobulinemia

Cryoglobulinemia is a rare

CTCL

 (CTCL) is a rare type of 

fanconi anemia

Essential Thrombocythemia

(ET) is a rare, chronic blood

Fanconi Anemia

 (FA) is a rare, inherited blood

Hairy Cell Leukemia

 (HCL) is a rare, slow-growing

hemoglobinopathies

Hemoglobinopathies

Hemoglobinopathies are a group

Hemophilia

Hemophilia is a rare genetic disorder

Hereditary Hemolytic Anemias

Hereditary hemolytic anemias are a

Hodgkin Lymphoma

Hodgkin lymphoma

Hodgkin lymphoma, also known as

Immune Thrombocytopenia (ITP)

Immune Thrombocytopenia (ITP)

(ITP) is a rare autoimmune

Hypereosinophilic Syndrome

Hypereosinophilic Syndrome

(HES) is a rare, chronic blood

Iron deficiency anemia

Iron deficiency anemia

Iron deficiency anemia is a common

Leukemia

Leukemia

Leukemia is a type of cancer

Lymphoma

Lymphoma

Lymphoma is a type of cancer

Macroglobulinemia

Macroglobulinemia

Macroglobulinemia is a rare 

MGUS

(MGUS)

Monoclonal Gammopathy of

Multiple Myeloma

Multiple Myeloma

Multiple Myeloma is a type of 

Myelodysplastic Syndromes (MDS)

(MDS)

Myelodysplastic Syndromes (MDS) are

Myelofibrosis

Myelofibrosis

Myelofibrosis is a rare type of bone

Myeloproliferative Disorders

Myeloproliferative Disorders

 (MPDs) are a group of rare blood 

Natural killer cell leukemia

Natural killer cell leukemia

(NK) Cell Leukemia is a rare and

Non-Hodgkin's Lymphoma

Non-Hodgkin's Lymphoma

(NHL) is a type of cancer that

Osteosclerotic Myeloma

Osteosclerotic Myeloma

Osteosclerotic Myeloma is a rare 

Paroxysmal Nocturnal Hemoglobinuria

Paroxysmal Nocturnal Hemoglobinuria

(PNH) is a rare, life-threatening

Pediatric Thrombocytopenia

Pediatric Thrombocytopenia

Pediatric Thrombocytopenia is a

Pediatric WBC Disorders

Pediatric White Blood Cell Disorders

Pediatric white blood cell disorders

POEMS Syndrome

POEMS Syndrome

POEMS syndrome is a rare,

Polycythemia Vera

Polycythemia Vera

Polycythemia Vera (PV) is a rare blood

Sickle Cell Anemia

Sickle Cell Anemia

Sickle Cell Anemia is a hereditary blood

Systemic Capillary Leak Syndrome

Systemic Capillary Leak Syndrome

Systemic Capillary Leak Syndrome, also

Systemic Mastocytosis

Systemic Mastocytosis

Systemic Mastocytosis is a rare 

Thalassemia

Thalassemia

Thalassemia is a genetic blood disorder

Thrombocytopenia (Low Platelet Count)

Thrombocytopenia

Thrombocytopenia is a medical 

Thrombocytosis

Thrombocytosis

Thrombocytosis is a condition

Vitamin Deficiency Anemia

Vitamin Deficiency Anemia

Vitamin Deficiency Anemia occurs 

Von Willebrand Disease

Von Willebrand Disease

 (VWD) is a genetic bleeding disorder

Waldenstrom Macroglobulinemia

Waldenstrom Macroglobulinemia

 (WM) is a rare form of cancer that

Low White Blood Cell Count (Leukopenia)

Low White Blood Cell Count

 (WBC) count drops below normal,

High White Blood Cell Count (Leukocytosis)

High White Blood Cell Count

Leukocytosis is a condition where the

Neutropenia

Neutropenia

Neutropenia is a condition 

Eosinophilia

Eosinophilia

Eosinophilia is a condition in which

Lymphocytopenia

Lymphocytopenia

Lymphocytopenia, also known as

Ewing Sarcoma

Ewing Sarcoma

Ewing Sarcoma is a rare and 

Hemophagocytic Lymphohistiocytosis (HLH)

(HLH)

(HLH) is a rare but life-threatening

Allogeneic Stem Cell Transplant

Allogeneic Stem Cell Transplant

(allo-SCT) is a life-saving treatment

Autologous Stem Cell Transplant

Autologous Stem Cell Transplant

Autologous Stem Cell Transplant is a

B-cell Lymphoma

B-cell Lymphoma

B-cell lymphoma is a type of

Heavy Chain Diseases

Heavy Chain Diseases

Heavy Chain Disease is a group of

Factor II, V, VII, X, or XII Deficiencies

Factor II, V, VII, X, or XII Deficiencies

Factor II, V, VII, X, and XII are proteins in

Blood clots

Blood clots

Blood clots are gel-like clumps of

Erythrocytosis

Erythrocytosis

Erythrocytosis is a medical condition 

Hypercoagulable Disorder

Hypercoagulable Disorder

also known as thrombophilia,

Basophilia

Basophilia

Basophilia is a condition characterized

Leucocytosis

Leucocytosis

Leucocytosis refers to an abnormally

Leucopenia

Leucopenia

Leucopenia is a medical condition

Monocytosis

Monocytosis

Monocytosis refers to an elevated level

Porphyria

Porphyria

Porphyria refers to a group of

Lymphocytosis

Lymphocytosis

Lymphocytosis is a condition

Thrombosis with thrombocytopenia syndrome (TTS)

(TTS)

Thrombosis with Thrombocytopenia

Immune thrombocytopenic purpura (ITP)

(ITP)

(ITP) is a blood disorder characterized

Leukopenia

Leukopenia

Leukopenia refers to an abnormal

Agranulocytosis

Agranulocytosis

Agranulocytosis is a serious blood 

Neutrophilia

Neutrophilia

Neutrophilia is a condition characterized

Chédiak–Higashi syndrome

Chédiak–Higashi syndrome

Chédiak–Higashi Syndrome (CHS) is

Cyclic neutropenia

Cyclic neutropenia

Cyclic Neutropenia is a rare blood 

Myeloid leukemia

Myeloid leukemia

Myeloid Leukemia is a type of blood

Bernard-Soulier Syndrome

Bernard-Soulier Syndrome

(BSS) is a rare genetic blood

Glanzmann's thrombasthenia

Glanzmann's thrombasthenia

Glanzmann’s Thrombasthenia is an 

Gray Platelet Syndrome

Gray Platelet Syndrome

 (GPS) is a rare, inherited blood

Bernard Soulier Disease

Bernard Soulier Disease

(BSS) is a rare, inherited bleeding

Hermansky Pudlak Syndrome

Hermansky Pudlak Syndrome

(HPS) is a rare, inherited genetic

Jacobsen Syndrome

Jacobsen Syndrome

Jacobsen Syndrome is a genetic

Lowe Syndrome

Lowe Syndrome

Lowe Syndrome, also known as 

Platelet release and storage pool defects

Platelet release and storage pool defects.

Platelet release and storage 

Acute Lymphoblastic Leukemia

Acute Lymphoblastic Leukemia

(ALL) is a fast-growing

Adrenoleukodystrophy

Adrenoleukodystrophy

(ALD) is a progressive 

Amegakaryocytosis & Congenital Thrombocytopenia

Amegakaryocytosis & Congenital

Amegakaryocytosis and congenital

Beta Thalassemia Major

Beta Thalassemia Major

Beta Thalassemia Major, often

Bone Marrow Failure Syndromes

Bone Marrow Failure Syndromes

Bone marrow is a soft, spongy

Chronic Leukemia

Chronic Leukemia

Chronic leukemia is a type of cancer

What is Hurler Syndrome (MPS-IH)

Hurler Syndrome (MPS-IH)

Hurler Syndrome is part of a group

Immune Deficiencies

Immune deficiencies are a group of

Inborn Errors of Metabolism

Inborn errors of metabolism are a

Juvenile Myelomonocytic Leukemia

Juvenile Myelomonocytic Leukemia

(JMML) is a rare and aggressive

Krabbe Disease (GLD)

Krabbe Disease (GLD)

Krabbe disease is a genetic disorder

Thrombocytopenia with absent radius (TAR) syndrome

(TAR)

(TAR) Syndrome is a rare genetic

Thrombotic thrombocytopenic purpura (TTP)

Thrombotic thrombocytopenic purpura

(TTP) is a rare and life-threatening

Metachromatic Leukodystrophy (MLD)

Metachromatic Leukodystrophy

 (MLD) is a rare, inherited genetic

Neuroblastoma

Neuroblastoma

Neuroblastoma is a type of cancer 

Plasma Cell Disorders

Plasma Cell Disorders

Plasma cell disorders refer to conditions

Pure Red Cell Aplasia

Pure Red Cell Aplasia

(PRCA) is characterized by the

Severe Combined Immunodeficiency

Severe Combined Immunodeficiency

(SCID) is a rare, life-threatening genetic

Sickle Cell Disease

Sickle Cell Disease

(SCD) is a hereditary blood disorder

Wiskott-Aldrich Syndrome

Wiskott-Aldrich Syndrome

Wiskott-Aldrich Syndrome is an X-linked

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