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Your search keyword '"Sarah Milla"' showing total 2 results
Start Over Author "Sarah Milla" Journal pediatrics and neonatology
2 results on '"Sarah Milla"'

1. Fetal and Postnatal Magnetic Resonance Imaging of Unilateral Cystic Renal Dysplasia in a Neonate with Tuberous Sclerosis

Author

Vineet Tyagi, Eran Bornstein, Robert Schacht, Shailee Lala, and Sarah Milla

Subjects
cystic renal disease, tuberous sclerosis, Pediatrics, RJ1-570
Abstract

Tuberous sclerosis (TS) is an autosomal dominant condition associated with mutations in the TSC1 and/or TSC2 genes. Clinical manifestations are multisystemic, and they often include lesions in the brain, skin, heart, kidneys, and bones. TSC2 gene mutations can be seen concomitantly with autosomal dominant polycystic kidney disease gene mutations. We present a case of a fetus with prenatal diagnosis of TS that had unique asymmetrical distribution of renal cystic disease. We describe the extensive work up with both fetal and neonatal magnetic resonance imaging with correlating images of the unilateral polycystic renal disease in addition to typical TS brain findings.

Published
2016
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2. Fetal and Postnatal Magnetic Resonance Imaging of Unilateral Cystic Renal Dysplasia in a Neonate with Tuberous Sclerosis

Author

Shailee V. Lala, Robert G. Schacht, Vineet Tyagi, Sarah Milla, and Eran Bornstein

Subjects
Adult, Pathology, medicine.medical_specialty, congenital, hereditary, and neonatal diseases and abnormalities, 030232 urology & nephrology, Autosomal dominant polycystic kidney disease, Prenatal diagnosis, tuberous sclerosis, Gene mutation, 03 medical and health sciences, Tuberous sclerosis, Fetus, 0302 clinical medicine, Prenatal Diagnosis, medicine, Humans, Pediatrics, Perinatology, and Child Health, medicine.diagnostic_test, business.industry, Infant, Newborn, lcsh:RJ1-570, Magnetic resonance imaging, lcsh:Pediatrics, Polycystic Kidney, Autosomal Dominant, medicine.disease, Magnetic Resonance Imaging, medicine.anatomical_structure, cystic renal disease, 030220 oncology & carcinogenesis, Mutation, Pediatrics, Perinatology and Child Health, Female, TSC1, TSC2, business
Abstract

Tuberous sclerosis (TS) is an autosomal dominant condition associated with mutations in the TSC1 and/or TSC2 genes. Clinical manifestations are multisystemic, and they often include lesions in the brain, skin, heart, kidneys, and bones. TSC2 gene mutations can be seen concomitantly with autosomal dominant polycystic kidney disease gene mutations. We present a case of a fetus with prenatal diagnosis of TS that had unique asymmetrical distribution of renal cystic disease. We describe the extensive work up with both fetal and neonatal magnetic resonance imaging with correlating images of the unilateral polycystic renal disease in addition to typical TS brain findings.

Published
2016

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