0000000000202602

AUTHOR

Enid F. Gilbert

showing 3 related works from this author

Chondrodysplasia punctata — Rhizomelic form

1976

Pathologic, ultrastructural and radiologic studies are described on 3 infants with the rhizomelic form of chondrodysplasia punctata. Radiologic criteria in the young infant include radiolucent coronal clefts dividing all or most of the thoracic and lumbar vertebral bodies, short humeri with flared metaphyses and punctate calcifications commonly present adjacent to the ossified ischial and pubic bones and less commonly in other locations. In late infancy and childhood the radiologic criteria include demineralization in all bones with slow maturation, flat vertebral bodies, short humeri and femora, metaphyseal flaring, especially in the distal humerus, proximal femur and proximal tibia, immat…

Cartilage ArticularMalemusculoskeletal diseasesChondrodysplasia PunctataPathologymedicine.medical_specialtyContractureDegeneration (medical)Skin DiseasesBone and BonesCataractInfant Newborn DiseasesLumbarmedicineHumansChondrodysplasia punctataFemurChildPelvisCerebral CortexNeuronsbusiness.industryCartilageMetaphyseal flaringInfant NewbornInfantPatellaAnatomyHumerusCystic Changemedicine.diseaseCartilagemedicine.anatomical_structureChild PreschoolPediatrics Perinatology and Child HealthMicrocephalyFemalePsychomotor DisordersbusinessCancellous boneEuropean Journal of Pediatrics
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Clinicopathological conference: an adolescent girl with severe mental impairment and mucopolysacchariduria.

1985

Pediatricsmedicine.medical_specialtyAdolescentbusiness.industrymedia_common.quotation_subjectMEDLINEMental impairmentMucopolysaccharidosesDiagnosis DifferentialMicroscopy ElectronMucopolysaccharidosis IIIIntellectual DisabilityMedicineHumansFemaleGirlbusinessGenetics (clinical)media_commonGlycosaminoglycansAmerican journal of medical genetics
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Studies of malformation syndromes of man XIB: the cerebro-hepato-renal syndrome of zellweger: Comparative pathology

1976

A study of 11 autopsied cases of the cerebro-hepato-renal syndrome of Zellweger (ZS) is reported. All cases had severe, persistent congenital hypotonia, hepatic lobular disarray, renal cortical cysts and pulmonary hypoplasia. Many had cardiovascular malformations, hepatomegaly, cerebral cortical gyral maldevelopment and pancreatic islet hyperplasia. Additional, less frequent findings are delineated. Results of iron content studies of hepatic and renal tissues are related to age of survival and possible development of fibrosis.

Heart Defects CongenitalLiver CirrhosisMalePathologymedicine.medical_specialtySiderosisCirrhosisRenal cortical cystsPancreatic islet hyperplasiaIronKidneyNeurologic ManifestationsPulmonary hypoplasiaMaldevelopmentFibrosisHumansMedicineAbnormalities MultipleRadiology Nuclear Medicine and imagingbusiness.industryInfant NewbornBrainInfantGeneral MedicineKidney Diseases Cysticmedicine.diseaseBile Ducts IntrahepaticNeonatal hypotoniaLiverConnective TissuePediatrics Perinatology and Child HealthFemaleHepatic fibrosisbusinessHepatomegalyEuropean Journal of Pediatrics
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