Search results for "Nephrosis"

showing 3 items of 33 documents

Congenital nephrosis, mesangial sclerosis, and distinct eye abnormalities with microcoria: An autosomal recessive syndrome

2004

We observed the occurrence of congenital nephrotic syndrome (CNS) and distinct ocular anomalies in two unrelated families. Eleven children from both families presented with a similar course of renal disease starting with nephrotic syndrome and renal failure prenatally or immediately after birth that resulted in death before the age of 2 months. Kidney histopathology showed diffuse mesangial sclerosis (DMS). Clinically obvious eye abnormalities were recognized in six of the eight patients in whom sufficient clinical data were available. Ocular anomalies included enlarged or large appearing corneae in some cases suggesting buphthalmos, and extremely narrow, nonreactive pupils (microcoria). Pa…

medicine.medical_specialtyPathologygenetic structuresbusiness.industryNephrosisGlomerulonephritisMicrocoriamedicine.diseaseeye diseasesLenticonusBuphthalmosEndocrinologyMaldevelopmentInternal medicineGeneticsmedicinesense organsbusinessCongenital nephrotic syndromeNephrotic syndromeGenetics (clinical)American Journal of Medical Genetics Part A
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Re: End Cutaneous Ureterostomy for the Management of Severe Hydronephrosis

2007

medicine.medical_specialtybusiness.industryureterostomyUrologymedicine.medical_treatmentUrinary diversionUrologymedicine.diseaseInfant newbornCutaneous ureterostomyUreterostomyUretermedicine.anatomical_structureReplantationmedicinebusinessHydronephrosisJournal of Urology
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The campomelic syndrome: review, report of 17 cases, and follow-up on the currently 17-year-old boy first reported by Maroteaux et al in 1971.

1983

We report 17 cases of the campomelic syndrome (CS) and a follow-up of one of the original patients of Maroteaux et al who is now 17 years old. Our review is based on 97 patients, including our own. An infant with the CS presents at birth with spectacularly short and bowed femora and tibiae. The initial chest radiograph confirms the diagnosis by demonstrating extremely small bladeless scapulae and hypoplastic pedicles of many thoracic vertebrae. Ossification of the sternal segments, pubis, talus, and knee epiphyses is also retarded. Usually the hips are dislocated and talipes equinovarus deformities are present. There is a small chondrocranium and a disproportionately large neurocranium. The…

musculoskeletal diseasesMaleAdolescentH-Y AntigenRespiratory SystemBone and BonesmedicineHumansAbnormalities MultipleGenitaliaHydronephrosisGenetics (clinical)Respiratory Distress Syndrome NewbornRespiratory distressmedicine.diagnostic_testOssificationbusiness.industryInfant NewbornAnatomySyndromemusculoskeletal systemmedicine.diseaseRenal hypoplasiaHypotoniaCampomelic dysplasiamedicine.anatomical_structureCartilageThoracic vertebraeFemalemedicine.symptomChest radiographbusinessAmerican journal of medical genetics
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