Treatments Archives | 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

(APS) is an autoimmune disorder

Benign Hematologic Conditions

Benign hematologic conditions are

Autoimmune Thrombocytopenia

also known as Immune

Autoimmune Hemolytic Anemias

Welcome to the specialized

Aplastic Anemia

Aplastic anemia is a rare and

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

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 are a group

Hemophilia

Hemophilia is a rare genetic disorder

Hereditary Hemolytic Anemias

Hereditary hemolytic anemias are a

Hodgkin lymphoma

Hodgkin lymphoma, also known as

Immune Thrombocytopenia (ITP)

(ITP) is a rare autoimmune

Hypereosinophilic Syndrome

(HES) is a rare, chronic blood

Iron deficiency anemia

Iron deficiency anemia is a common

Leukemia

Leukemia is a type of cancer

Lymphoma

Lymphoma is a type of cancer

Macroglobulinemia

Macroglobulinemia is a rare

(MGUS)

Monoclonal Gammopathy of

Multiple Myeloma

Multiple Myeloma is a type of

(MDS)

Myelodysplastic Syndromes (MDS) are

Myelofibrosis

Myelofibrosis is a rare type of bone

Myeloproliferative Disorders

(MPDs) are a group of rare blood

Natural killer cell leukemia

(NK) Cell Leukemia is a rare and

Non-Hodgkin's Lymphoma

(NHL) is a type of cancer that

Osteosclerotic Myeloma

Osteosclerotic Myeloma is a rare

Paroxysmal Nocturnal Hemoglobinuria

(PNH) is a rare, life-threatening

Pediatric Thrombocytopenia

Pediatric Thrombocytopenia is a

Pediatric White Blood Cell Disorders

Pediatric white blood cell disorders

POEMS Syndrome

POEMS syndrome is a rare,

Polycythemia Vera

Polycythemia Vera (PV) is a rare blood

Sickle Cell Anemia

Sickle Cell Anemia is a hereditary blood

Systemic Capillary Leak Syndrome

Systemic Capillary Leak Syndrome, also

Systemic Mastocytosis

Systemic Mastocytosis is a rare

Thalassemia

Thalassemia is a genetic blood disorder

Thrombocytopenia

Thrombocytopenia is a medical

Thrombocytosis

Thrombocytosis is a condition

Vitamin Deficiency Anemia

Vitamin Deficiency Anemia occurs

Von Willebrand Disease

(VWD) is a genetic bleeding disorder

Waldenstrom Macroglobulinemia

(WM) is a rare form of cancer that

Low White Blood Cell Count

(WBC) count drops below normal,

High White Blood Cell Count

Leukocytosis is a condition where the

Neutropenia

Neutropenia is a condition

Eosinophilia

Eosinophilia is a condition in which

Lymphocytopenia

Lymphocytopenia, also known as

Ewing Sarcoma

Ewing Sarcoma is a rare and

(HLH)

(HLH) is a rare but life-threatening

Allogeneic Stem Cell Transplant

(allo-SCT) is a life-saving treatment

Autologous Stem Cell Transplant

Autologous Stem Cell Transplant is a

B-cell Lymphoma

B-cell lymphoma is a type of

Heavy Chain Diseases

Heavy Chain Disease is a group of

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

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

Blood clots

Blood clots are gel-like clumps of

Erythrocytosis

Erythrocytosis is a medical condition

Hypercoagulable Disorder

also known as thrombophilia,

Basophilia

Basophilia is a condition characterized

Leucocytosis

Leucocytosis refers to an abnormally

Leucopenia

Leucopenia is a medical condition

Monocytosis

Monocytosis refers to an elevated level

Porphyria

Porphyria refers to a group of

Lymphocytosis

Lymphocytosis is a condition

(TTS)

Thrombosis with Thrombocytopenia

(ITP)

(ITP) is a blood disorder characterized

Leukopenia

Leukopenia refers to an abnormal

Agranulocytosis

Agranulocytosis is a serious blood

Neutrophilia

Neutrophilia is a condition characterized

Chédiak–Higashi syndrome

Chédiak–Higashi Syndrome (CHS) is

Cyclic neutropenia

Cyclic Neutropenia is a rare blood

Myeloid leukemia

Myeloid Leukemia is a type of blood

Bernard-Soulier Syndrome

(BSS) is a rare genetic blood

Glanzmann's thrombasthenia

Glanzmann’s Thrombasthenia is an

Gray Platelet Syndrome

(GPS) is a rare, inherited blood

Bernard Soulier Disease

(BSS) is a rare, inherited bleeding

Hermansky Pudlak Syndrome

(HPS) is a rare, inherited genetic

Jacobsen Syndrome

Jacobsen Syndrome is a genetic

Lowe Syndrome

Lowe Syndrome, also known as

Platelet release and storage pool defects.

Platelet release and storage

(TAR)

(TAR) Syndrome is a rare genetic

(TTP)

Thrombotic Thrombocytopenic Purpura

ثلاسيميا، أعراضه و تشخيصه و علاجه

الثلاسيميا هو اضطراب وراثي في الدم يتميز بعدم قدرة الجسم على إنتاج كمية كافية من الهيم

التصلب العصبي المتعدد

التصلب العصبي المتعدد هو اضطراب مناعي مزمن حيث يهاجم جهاز المناعة عن طريق الخطأ الجهاز ا