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20 Possible Causes for Congenital Malformation of the Ribs, Protein-Losing Enteropathy

  • Juvenile Polyposis Syndrome

    We report an unusual case of JPS associated with massive gastric polyposis, resulting in a giant stomach, severe anemia, hematemesis, protein-losing enteropathy, and gastric[] , Neoplasia (basal cellcarcinoma, ovarian carcinoma, medulloblastoma). (GS) may present in infancy with congenital hydrocephalus, cleft lip and palate, lungcysts, rib and[] Potential complications from Juvenile Polyposis Syndrome include: A condition known as protein-losing enteropathy in children (loss of protein owing to diarrhea) Growth retardation[]

  • Skeletal Dysplasia

    She presented with protein-losing enteropathy in her 6th month. Post-mortem examination revealed lymphangiectasia in the small intestine.[] […] with congenital malformations, such as the short-rib polydactyly group 15 ( Table 1 ).[] Protein-losing enteropathy is a primary or secondary manifestation of a group of conditions, and etiologies which are broadly divisible into those with mucosal injury on the[]

  • Noonan Syndrome

    There are few reports on successful high-dose spironolactone treatment of refractory protein-losing enteropathy (PLE) caused by Fontan procedure.[] Specialty Medical genetics, pediatrics Symptoms Mildly unusual facial features, short height, congenital heart disease, bleeding problems, skeletal malformations [1] Complications[] Protein-losing enteropathy (PLE) developing in Noonan syndrome is rare.[]

  • Thanatophoric Dysplasia

    Dehner, Proteinlosing enteropathy with intestinal lymphangiectasia in skeletal dysplasia with Lys650Met mutation, American Journal of Medical Genetics Part A, 170, 11, (2993[] malformations of spine, not associated with scoliosis Q76.6 Other congenital malformations of ribs Q76.7 Congenital malformation of sternum Q76.8 Other congenital malformations[] […] of bony thorax Q76.9 Congenital malformation of bony thorax, unspecified Q77 Osteochondrodysplasia with defects of growth of tubular bones and spine Q77.0 Achondrogenesis[]

  • Isolated Congenital Alacrima

    Manifestations range from mild to severe, involving only protein-losing enteropathy and hypoglycemia or severe intellectual disability with malfunction of several organs.[] […] ovarian fibroma Medulloblastoma Lymphomesenteric cysts Congenital malformation: cleft lip and/or palate, polydactyly, congenital ocular anomaly (cataract, microphthalmos,[] Cardiomyopathy Neoplasm Pleural lymphangiectasia Pericardial lymphangiectasia Thyroid lymphangiectasia Mild postnatal growth retardation Conical incisor Severe hydrops fetalis Protein-losing[]

  • Coxoauricular Syndrome

    CFDD OMIM:609814 Complement Factor H Deficiency; CFHD OMIM:610984 Complement Factor I Deficiency; CFID OMIM:226300 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing[] […] in the male: A new X-linked dominant multiple congenital anomalies syndrome?[] Thoracic Dysplasia 10 with or Without Polydactyly 41 626 c CNG187 Congenital Disorder of Glycosylation, Type Iid 41 627 ISL121 Isolated Split Hand-Split Foot Malformation[]

  • Congenital Clubbing

    Protein losing enteropathy In protein-losing enteropathy (PLE) loss of protein in the bowel, secondary to lymphatic distension may be due to elevated systemic venous pressure[] Other congenital anomalies outside the genitourinary system are musculoskeletal (hemivertebrae, scoliosis, rib defects, clubfoot, congenital hip dislocation), cardiovascular[] Rao PS (2007) Protein-losing enteropathy following the Fontan operation. J Invasive Cardiol 19: 447-448.[]

  • Familial Congenital Nasolacrimal Duct Obstruction

    C Deficiency Protein Deficiency Protein S Deficiency Protein-Energy Malnutrition Protein-Losing Enteropathies Proteinuria Proteus Infections Proteus Syndrome Protozoan Infections[] […] ovarian fibroma Medulloblastoma Lymphomesenteric cysts Congenital malformation: cleft lip and/or palate, polydactyly, congenital ocular anomaly (cataract, microphthalmos,[] Prosopagnosia Prostatic Diseases Prostatic Hyperplasia Prostatic Intraepithelial Neoplasia Prostatic Neoplasms Prostatitis Prosthesis Failure Prosthesis-Related Infections Protein[]

  • Congenital Absence of Thigh and Lower Leg with Foot Present

    Serum albumin was checked to rule out other etiologies of hypoalbuminemia (eg, protein-losing enteropathy and kwashiorkor).[] ribs Accessory rib Congenital: · absence of rib · fusion of ribs · malformation of ribs NOS Excludes: short rib syndrome ( Q77.2 ) Q76.7 Congenital malformation of sternum[] malformations of spine, not associated with scoliosis Q765Cervical rib Q766Other congenital malformations of ribs Q767Congenital malformation of sternum Q768Other congenital[]

  • Schneckenbecken Dysplasia

    losing enteropathy, Waldmann disease, Whipple's disease Genetic Aagenaes syndrome, amnion rupture sequence, Andersen disease, aplasia cutis congenital - intestinal lymphangiectasia[] […] with congenital malformations, such as the short-rib polydactyly group 15 ( Table 1 ).[] […] cirrhosis, hepatic failure, hepatic venous obstruction, hepatitis, liver disease, liver failure, malabsorption syndrome, Ménétrier's disease, primary biliary cirrhosis, protein[]

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