Infantile myofibromatosis: a rare cause of subcutaneous nodules in an infant
Arch Dis Child
.
2020 Jun 23:archdischild-2020-319229.
doi: 10.1136/archdischild-2020-319229.
Online ahead of print.
Authors
Gerarda Mastrogiorgio
1
,
Paola Sabrina Buonuomo
2
,
Ippolita Rana
2
,
Marina Macchiaiolo
2
,
Paola Marchetti
3
,
Francesco De Peppo
3
,
Martina Rinelli
4
,
Michaela Veronika Gonfiantini
2
,
Antonio Novelli
4
,
Andrea Bartuli
2
Affiliations
1
Rare Diseases and Medical Genetics, Bambino Gesu Pediatric Hospital, Roma, Lazio, Italy gerarda.mastrogiorgio@opbg.net.
2
Rare Diseases and Medical Genetics, Bambino Gesu Pediatric Hospital, Roma, Lazio, Italy.
3
Pediatric Surgery, Bambino Gesu Pediatric Hospital, Roma, Lazio, Italy.
4
Medical Genetics Laboratory, Bambino Gesu Pediatric Hospital, Roma, Lazio, Italy.
PMID:
32576562
DOI:
10.1136/archdischild-2020-319229
No abstract available
Keywords:
genetics; patient care team.