Total anomalous pulmonary venous connection and a constellation of craniofacial, skeletal, and urogenital anomalies in a newborn and similar features in his 36-year-old father

Clinical Dysmorphology

Volumn 10, Issue 2, 2001, Pages 95-99

  Pierson, Diane M ^a,b   Taboada, Eugenio M ^a,b   Lofland, Gary K ^a,b   Begleiter, Michael L ^a,b   Smith, Gregory S ^a,b   Hall, Frederick ^a,b   Butler, Merlin G ^a,b  

^a CHILDREN S MERCY HOSPITAL   (United States)

^b UNIVERSITY OF MISSOURI KANSAS CITY SCHOOL OF MEDICINE   (United States)

Author keywords

Autosomal dominant; Brachyphalangy; Craniofacial anomalies; Micropenis; Preaxial polydactyly; Tibial shortening; Total anomalous pulmonary connection

Indexed keywords

ARTICLE; AUTOPSY; AUTOSOMAL DOMINANT INHERITANCE; CASE REPORT; CLINICAL EXAMINATION; CRANIOFACIAL MALFORMATION; FATHER CHILD RELATION; HORSESHOE KIDNEY; HUMAN; LUNG VEIN DRAINAGE ANOMALY; MALE; MALFORMATION SYNDROME; MICROPENIS; NEWBORN; POLYDACTYLY; PRIORITY JOURNAL; SYNDROME DELINEATION;

EID: 0035085237     PISSN: 09628827     EISSN: None     Source Type: Journal    
DOI: 10.1097/00019605-200104000-00004     Document Type: Article

References (1)

1. A syndrome of brachyphalangy, polydactyly and absent tibiae