Renomegaly: Causes & Reasons

Possible Causes for Renomegaly

Glycogen storage disease type I (GSDI) is characterized by accumulation of glycogen and fat in the liver and kidneys, resulting in hepatomegaly and renomegaly. [ncbi.nlm.nih.gov]

Most common type of GSD I: Ia ( > 80%) Onset: Before 1 yr Clinical features: Before 1 yr, severe hypoglycemia, lactic acidosis, and hepatomegaly; later, hepatic adenomas, renomegaly [msdmanuals.com]

[…] at bedtime Fanconi-Bickel syndrome (227810) Glucose transporter-2 GLUT2 (3q26)* Onset: Infancy Clinical features: Failure to thrive, abdominal distention, hepatomegaly, renomegaly [msdmanuals.com]

Fanconi-Bickel Syndrome

We report a 3-year-old boy from southern India who presented with doll-like facies, florid rickets, massive hepatomegaly, growth retardation, renomegaly and laboratory evidence [scinapse.io]

Glycogen Storage Disease Type 1

[…] disease (or Hepatorenal Glycogenosis or Glycogen Storage Disease Type I a) which is also characterized by growth retardation, "doll-like" face, massive hepatomegaly and renomegaly [indianpediatrics.net]

Beckwith-Wiedemann Syndrome

[…] birth Minor features: Creases at the earlobes, blood vessel defect called port-wine stain (often seen as a red birthmark), low blood sugar (hypoglycemia), enlarged kidney (renomegaly [dovemed.com]

Diabetes Mellitus Type 1

Type 1 diabetes is an autoimmune disease that gradually destructs insulin-producing beta cells. Over the years, clinicians' knowledge regarding the immunopathogenesis of this disease has greatly increased. Immunotherapies that can change the course of immune-mediated destruction and preserve and possibly regenerate[…] [ncbi.nlm.nih.gov]

Lymphoma

Overview Lymphoma is a broad term for cancer that begins in cells of the lymph system. The two main types are Hodgkin lymphoma and non-Hodgkin lymphoma (NHL). Hodgkin lymphoma can often be cured. The prognosis of NHL depends on the specific type. Explore the links on this page to learn more about lymphoma[…] [cancer.gov]

Nephroblastoma

You are here Home > Types of Cancer > Wilms Tumor - Childhood Wilms Tumor - Childhood This is Cancer.Net’s Guide to Wilms Tumor - Childhood. Use the menu below to choose the Introduction section to get started. Or, you can choose another section to learn more about a specific question you have. Each guide is[…] [cancer.net]

Lymphomatoid Granulomatosis

Lymphomatoid granulomatosis Infobox_Disease Name = PAGENAME Caption = DiseasesDB = 33208 ICD10 = ICD9 = ICDO = 9766/1 OMIM = MedlinePlus = eMedicineSubj = med eMedicineTopic = 1369 MeshID = D008230 Lymphomatoid granulomatosis is a neoplastic disease. It is a lymphoproliferative disorder (lymphomatoid means[…] [enacademic.com]

Congenital Disorder of Glycosylation Type 1B

INHERITANCE: autosomal recessive Glycogen storage disease Type 1A (GSD1A) is a metabolic condition that when untreated, often results in severe hypoglycemia, seizures, hepato- and renomegaly [chginc.org]

Ochoa Syndrome

Journal List Einstein (Sao Paulo) v.13(2); Apr-Jun 2015 PMC4943824 Einstein (Sao Paulo). 2015 Apr-Jun; 13(2): 279–282. Full-text translation available in Portuguese. Abstract Ochoa syndrome is rare and its major clinical problems frequently unrecognized. We describe facial characteristics of six patients to help[…] [ncbi.nlm.nih.gov]

Polycystic Kidney Disease

Nat Commun. 2018 Feb 26;9(1):814. doi: 10.1038/s41467-018-03036-y. Author information 1 Departments of Molecular Biology and Internal Medicine, UT Southwestern Medical Center, Dallas, TX, 75390, USA. 2 Children's Medical Center Research Institute at UTSW, Eugene McDermott Center for Human Growth & Development,[…] [ncbi.nlm.nih.gov]

Nephronophthisis 16

Symbol Name Synonyms Organism NPHP1 nephronophthisis 1 (juvenile) FLJ97602, JBTS4, Juvenile nephronophthisis 1 protein, Nephrocystin-1, NPH1, SLSN1 Homo sapiens WikiGenes edit this page UniProt O15259, O14837, C9J082 IntAct O15259 PDB Structure 1S1N OMIM 607100, 609583 NCBI Gene 4867 NCBI RefSeq NP_000263, NP_001121650[…] [ihop-net.org]

Saldino-Noonan Syndrome

SRPS1, like SRPS2, is a lethal condition in the newborn period or autosomal recessive inheritance. The infant has a hydropic appearance, postaxial polydactyly, severely shortened and flipper-like limbs, and striking metaphyseal dysplasia of tubular bones. Ossification is defective in the calvaria, vertebrae, pelvis, and[…] [humpath.com]

Mucopolysaccharidosis-plus Syndrome

Desarrollado de la mano de expertos clínicos del mundo de la reproducción y de la genética. Porque lo que realmente nos importa es contribuir a que tengamos niños sanos nuestro test qCarrier Plus minimiza al máximo el riesgo residual de cada uno de los más de 300 genes estudiados. Ver lista de genes Un test de[…] [qgenomics.com]

Malignant Kidney Neoplasm

Hereditary Amyloidosis

Amiloidosi ATTR ereditaria: una malattia familiare progressiva e potenzialmente letale1-3 Bibliografia: Adams D, Coelho T, Obici L, et al. Rapid progression of familial amyloidotic polyneuropathy: a multinational natural history study. Neurology. 2015;85(8):675-682. Hanna M. Novel drugs targeting transthyretin amyloidosis.[…] [hattramyloidosis.it]

Renon-Delille Syndrome

[…] renointestinal renointestinal reflex Renoir Renoir,Pierre Auguste Renoiresque renolin renomado renombrado renombre renome renomear renomedullar interstitial cell renomedullary lipid renomegaly [zh-cn.oldict.com]

[…] syndrome」の関連用語 1 雷-德二氏综合征中英英中専門用語 100% テキスト翻訳 >> Weblio翻訳中国語⇒日本語日本語⇒中国語 Renon-Delille syndromeのお隣キーワード renointestinal reflex Renolumbar artery Reno-M renomedullary lipid renomegaly [cjjc.weblio.jp]

Tyrosinemia Type 1

RESUMEN La tirosinemia de tipo I es un error innato del metabolismo de aminoácidos, ocasionada por la deficiencia o ausencia de la actividad enzimática de la hidrolasa del fumarilacetoacetato del catabolismo de tirosina; con un cuadro clínico variable, se puede manifestar desde una forma neonatal grave hasta una[…] [elsevier.es]

Glycogen Storage Disease Type 1B

Fonti utilizzate nella revisione corrente Reviewed January 2016 by Peter L. Platteborze, PhD, DABCC, FACB, Laboratory Director. (May 2013 reviewed) KidsHealth.org. G6PD Deficiency.Available online at http://m.kidshealth.org/parent/general/aches/g6pd.html.Accessed on 1/24/2016. (Reviewed May 2006) Genetics Home[…] [labtestsonline.it]

Renal-Hepatic-Pancreatic Dysplasia 1

Atlas of Genetics and Cytogenetics in Oncology and Haematology Home Genes Leukemias Solid Tumors Cancer-Prone Deep Insight Case Reports Journals Portal Teaching X Y 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 NA NPHP3-ACAD11 (NPHP3-ACAD11 readthrough (NMD candidate)) Identity Other alias - HGNC (Hugo)[…] [atlasgeneticsoncology.org]

Lethal Congenital Glycogen Storage Disease of the Heart

Congenital Disorder of Glycosylation Type 1A

Case Reports Underdiagnosis of mild congenital disorders of glycosylation type Ia Irina Giurgea et al. Pediatr Neurol. 2005 Feb. Abstract Congenital disorders of glycosylation-Ia are the most frequent type of congenital disorders of glycosylation. This condition affects the nervous system as well as other organs. The[…] [pubmed.ncbi.nlm.nih.gov]

Phosphoglycerate Kinase 1 Deficiency

 Renomegaly.  Spleen normal.  Bleeding tendency.  Skin xanthomas.  Gouty arthritis.  patients with GSD Ib develop neutropenia.  GSD Ib patients show symptoms of inflammatory [slideshare.net]

Lesser Sac Abscess

You can see calcification in less than 50% of the ureters, associated to a renomegaly. [marcosgodoy.com]

You can see a diffused calcification in the kidney, associated to a severe renomegaly. [marcosgodoy.com]

You can see calcification in less than 50% of the renal tubules, paleness and posterior renomegaly. [marcosgodoy.com]

Glycogen Storage Disease Type 10

Liver Glycogen Synthase Deficiency

Pelvic Hematoma

Pathologic findings include massive subepithelial and peripelvic hemorrhage, hydronephrosis, cortical infarcts, and renomegaly. [ncbi.nlm.nih.gov]

Disorders of Pyruvate Metabolism and Gluconeogenesis

Muscle Phosphorylase Kinase Deficiency

Hirschsprung Disease - Nail Hypoplasia - Dysmorphism

At autopsy, findings were right CDH, severe pulmonary hypoplasia, atresia of the esophagus and proximal duodenum, renomegaly (combined weight 34.1 g; average for gestation [nature.com]