An unusual case of nephrotic syndrome in a microcephalic infant: Questions

Pediatr Nephrol. 2019 Nov;34(11):2325-2326. doi: 10.1007/s00467-019-04260-4. Epub 2019 May 8.

Authors

Elizabeth Baker¹, Donald Weaver¹, Susan Massengill¹, Dana Mittag¹, Jane Juusola², Laurie Demmer³

Affiliations

¹ Atrium Health's Levine Children's Hospital, 1000 Blythe Blvd, Charlotte, NC, 28203, USA.
² GeneDx, 207 Perry Pkwy, Gaithersburg, MD, 20877, USA.
³ Atrium Health's Levine Children's Hospital, 1000 Blythe Blvd, Charlotte, NC, 28203, USA. laurie.demmer@atriumhealth.org.

PMID: 31069510
DOI: 10.1007/s00467-019-04260-4

No abstract available

Keywords: Microcephaly; Nephrotic syndrome.

Publication types

Case Reports

MeSH terms

Chromosome Deletion*
Chromosomes, Human, Pair 14 / genetics
Chromosomes, Human, Pair 8 / genetics
Failure to Thrive / complications
Failure to Thrive / diagnosis*
Failure to Thrive / genetics
Fatal Outcome
Genetic Testing
Humans
Infant
Male
Microcephaly / complications
Microcephaly / diagnosis*
Microcephaly / genetics
Nephrotic Syndrome / complications
Nephrotic Syndrome / diagnosis*
Nephrotic Syndrome / genetics
Nephrotic Syndrome / therapy