Heterotaxia in a fetus with campomelia, cervical lymphocele, polysplenia, and multicysctic dysplastic kidneys: Expanding the phenotype of Cumming syndrome

American Journal of Medical Genetics

Volumn 73, Issue 4, 1997, Pages 419-424

  Ming, Jeffrey E ^a,b   McDonald McGinn, Donna M ^a   Markowitz, Richard I ^a   Ruchelli, Eduardo ^a   Zackai, Elaine H ^a  

^a UNIVERSITY OF PENNSYLVANIA   (United States)

^b CHILDREN S HOSPITAL OF PHILADELPHIA   (United States)

Author keywords

Campomelia; Cumming syndrome; Heterotaxia; Polyasplenia

Indexed keywords

ACCESSORY SPLEEN; AORTA ARCH ANOMALY; ARTICLE; CASE REPORT; CONGENITAL BLOOD VESSEL MALFORMATION; DEXTROCARDIA; FEMALE; FETUS; HUMAN; KIDNEY POLYCYSTIC DISEASE; LIMB MALFORMATION; LUNG MALFORMATION; LUNG VEIN DRAINAGE ANOMALY; LYMPHOCELE; PHENOTYPE; PRIORITY JOURNAL; SUPERIOR CAVA VEIN; SYNDROME;

ABNORMALITIES, MULTIPLE; BONE AND BONES; FEMALE; FETAL DISEASES; HEART DEFECTS, CONGENITAL; HUMANS; LUNG; POLYCYSTIC KIDNEY DISEASES; PREGNANCY; SPLEEN; SYNDROME; VISCERA;

GENETTA;

EID: 0030778070     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: None     Document Type: Article

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