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Medical condition in which organs are larger than normal
Organomegaly is the abnormal enlargement of organs. For example, cardiomegaly is enlargement of the heart. Visceromegaly is the enlargement of abdominal
Organomegaly
Paraneoplastic syndrome
for some of the disease's major signs and symptoms (polyneuropathy, organomegaly, endocrinopathy, myeloma protein, and skin changes), as is PEP (polyneuropathy
POEMS_syndrome
Rare human systemic disease
initials of thrombocytopenia, anasarca, fever, reticulin fibrosis and organomegaly. It was first described, in three patients, in 2010 by Takei et al, and
TAFRO_syndrome
Cancer of plasma cells
produce symptoms, e.g., AL amyloidosis), and peripheral neuropathy, organomegaly, endocrinopathy, monoclonal plasma cell disorder, and skin changes. In
Multiple_myeloma
Group of lymphoproliferative disorders
cell population found in patients with POEMS syndrome (polyneuropathy, organomegaly, endocrinopathy, monoclonal plasma cell disorder, and skin changes) can
Castleman_disease
Medical condition
for sJIA include arthritis, ≥2 weeks of daily fever, and symptoms like organomegaly, lymphadenopathy, serositis, or non-fixed/evanescent rash. Laboratory
Systemic-onset juvenile idiopathic arthritis
Systemic-onset_juvenile_idiopathic_arthritis
Blood cancer characterized by overproduction of lymphoblasts
Favorable Age <2 or >10 years 3–5 years Sex Male Female Race Black Caucasian Organomegaly Present Absent Mediastinal mass Present Absent CNS involvement Present
Acute_lymphoblastic_leukemia
Indications of a specific illness, including psychiatric
rattle (last moments of life) Hemoptysis (blood-stained sputum) Jaundice Organomegaly an enlarged organ such as the liver (hepatomegaly) Palmar erythema (reddening
Signs_and_symptoms
Medical condition
loss loss of appetite fatigue pallor easy bruising frequent infections organomegaly Similar to other subtypes of AML, sporadic cases of ABL typically arise
Acute_basophilic_leukemia
porokeratosis (classic porokeratosis, porokeratosis of Mibelli) Polyneuropathy–organomegaly–endocrinopathy–monoclonal gammopathy–skin changes syndrome (Crow–Fukase
List_of_skin_conditions
Rare metabolic genetic disorder resulting in leukoencephalopathy
mild spasticity, optic atrophy, and a sensorimotor neuropathy, without organomegaly or dysfunction of internal organs. MRI scans performed at ages eleven
Ribose-5-phosphate isomerase deficiency
Ribose-5-phosphate_isomerase_deficiency
Congenital disorder
symptons:[citation needed] Macrosomia Macroglossia Advanced bone age Organomegaly is especially noted in liver and spleen malformations of the kidneys
Simpson–Golabi–Behmel syndrome
Simpson–Golabi–Behmel_syndrome
Hematological malignancy
hemoglobin, absolute neutrophil count, and platelet count), symptomatic organomegaly, recurrent infections, or constitutional symptoms. This watchful waiting
Hairy_cell_leukemia
Abnormally elevated levels of lipids or lipoproteins in the blood
Complications include retinal vein occlusion, acute pancreatitis, steatosis, and organomegaly, and lipemia retinalis. Hyperlipoproteinemia type II is further classified
Hyperlipidemia
Inflammation of the fatty layer under the skin (panniculus adiposus)
tender erythematous nodules, recurrent high fever, malaise, jaundice, organomegaly, serosal effusions, pancytopenia, hepatic dysfunction and coagulation
Panniculitis
Clinical examination technique
used to find whether any organ is enlarged and similar (assessing for organomegaly). It is based on the principle of setting tissue and spaces in between
Percussion_(medicine)
Medical condition
circulating monoclonal B-cells; 2) lack evidence of lymphadenopathy, organomegaly, or other tissue involvements caused by these cells; 3) no features of
Monoclonal B-cell lymphocytosis
Monoclonal_B-cell_lymphocytosis
Physical examination of abdomen
pain on the surface. On deep palpation, the examiner is testing for any organomegaly (enlarged organs.) Typically, the clinician is looking for enlargement
Abdominal_examination
testing POD postoperative days POEMS POEMS syndrome (polyneuropathy, organomegaly, endocrinopathy, myeloma protein and skin changes) POLST Physician Orders
List of medical abbreviations: P
List_of_medical_abbreviations:_P
Autoimmune disease affecting the peripheral nervous system
Myelin-associated glycoprotein-associated gammopathy, polyneuropathy, organomegaly, endocrinopathy, M-protein and skin changes syndrome (POEMS) Other possible
Chronic inflammatory demyelinating polyneuropathy
Chronic_inflammatory_demyelinating_polyneuropathy
Medical condition
with thrombocytopenia, anasarca, myelofibrosis, renal dysfunction, and organomegaly syndrome (TAFRO syndrome) are considered to have a distinct clinical
Idiopathic multicentric Castleman disease
Idiopathic_multicentric_Castleman_disease
Protein-coding gene in the species Homo sapiens
postnatal growth restriction, reduced bone and skeletal muscle growth, and organomegaly. Expression of this gene is induced by estrogen and altered in some breast
STC2
Medical condition
osteitis Organic dust toxic syndrome Panniculitis POEMS (polyneuropathy, organomegaly, endocrinopathy, monoclonal protein, skin changes) Polymer fume fever
Fever_of_unknown_origin
Genetic overgrowth disorder
the common symptoms of BWS. These symptoms may include macroglossia, organomegaly, periorbital fullness, and hernias. Knockout models for CDKN1C in mice
Beckwith–Wiedemann_syndrome
Medical condition
difficult. The most common features include Immune dysregulation (95%) Organomegaly (86%) Recurrent infections (71%) Hypogammaglobulinemia (57%) Granulomatous
LPS-responsive beige-like anchor protein deficiency
LPS-responsive_beige-like_anchor_protein_deficiency
Medical diagnostic method
urinated within 1 hour before the procedure Patients with bladder cancer Organomegaly or other intraabdominal organ abnormalities Overlying soft tissue infections
Suprapubic_aspiration
Medical condition
disorder. Some infants with Sandhoff disease may have enlarged organs (organomegaly) or bone abnormalities. Children with the severe form of this disorder
Sandhoff_disease
irregularities: adrenocorticoid hypersecretion enlarged pituitary and adrenal gland size (organomegaly) elevated corticotropin-releasing factor (CRF) concentrations
Differential diagnoses of depression
Differential_diagnoses_of_depression
Spectrum of blood disorders
the characteristic signs or symptoms of the syndrome: Polyneuropathy, Organomegaly, Endocrinopathy, Plasma cell disorder (typically, the plasma cell burden
Plasma_cell_dyscrasias
Species of bacterium
can still survive in an anaerobic environments. Infection can cause organomegaly, ocular disease, rectal prolapse, ecchymosis, and erosions on the skin
Edwardsiella_tarda
Death of domestic cattle
various tissues, leading to macroglossia, macrosomia, enlarged organs (organomegaly), umbilical hernias, omphaloceles, hypoglycemia, ear malformations, and
Cow_mortality
Medical condition
lymphomas can present with a variety of clinical symptoms, including organomegaly, lymphadenopathy, and/or constitutional symptoms. Unknown fever, cytopenias
AIDS-related_lymphoma
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