Familial multiple ventricular extrasystoles, short stature, craniofacial abnormalities and digital hypoplasia: A further case of Stoll syndrome?

Clinical Dysmorphology

Volumn 17, Issue 2, 2008, Pages 91-93

  Mercer, Catherine L ^a,b   Keeton, Barry ^a,b   Dennis, Nicolas R ^a,b  

^a PRINCESS ANNE HOSPITAL   (United Kingdom)

^b SOUTHAMPTON GENERAL HOSPITAL   (United Kingdom)

Author keywords

Autosomal dominant; Brachydactyly; Dental abnormalities; Micrognathia; Ventricular extrasystoles

Indexed keywords

ARTICLE; BRACHYDACTYLY; CASE REPORT; CRANIOFACIAL MALFORMATION; DIGITAL HYPOPLASIA; DOMINANT INHERITANCE; ECHOCARDIOGRAPHY; FAMILIAL MULTIPLE VENTRICULAR EXTRASYSTOLE; FAMILY; FINGER MALFORMATION; GENETIC ASSOCIATION; HEART VENTRICLE EXTRASYSTOLE; HUMAN; INTERPHALANGEAL JOINT; MALE; PHENOTYPE; PIERRE ROBIN SYNDROME; PRIORITY JOURNAL; RELATIVE; SCHOOL CHILD; SHORT STATURE; SIBLING; STOLL SYNDROME;

ABNORMALITIES, MULTIPLE; ADOLESCENT; ADULT; BODY HEIGHT; CHILD; CRANIOFACIAL ABNORMALITIES; FACIES; FEMALE; FINGER PHALANGES; HUMANS; MALE; MICROGNATHISM; PEDIGREE; SYNDROME; VENTRICULAR PREMATURE COMPLEXES;

EID: 41849125673     PISSN: 09628827     EISSN: None     Source Type: Journal    
DOI: 10.1097/MCD.0b013e3282efefc9     Document Type: Article

References (1)

1. Stoll C, Kieny J, Dott B, Alembik Y, Finck S (1992). Ventricular extrasystoles with syncopal episodes, perodactyly, and Robin sequence in three generations. Am J Med Genet 42:480-486.