Cumming syndrome: Report of two additional cases

Pediatric Radiology

Volumn 28, Issue 10, 1998, Pages 798-801

  Dibbern, Kurt M ^a,b   Graham, John M ^a   Lachman, Ralph S ^a,b,c   Wilcox, William R ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b HARBOR UCLA MEDICAL CENTER   (United States)

^c Intl Skeletal Dysplasia Registry   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BONE MALFORMATION; CASE REPORT; CONFERENCE PAPER; CUMMING SYNDROME; FEMALE; FETUS; HUMAN; LONG BONE; LYMPHOCELE; PRIORITY JOURNAL; RADIOLOGY;

ABNORMALITIES, MULTIPLE; BONE AND BONES; FEMALE; FEMUR; FETAL DISEASES; HEART DEFECTS, CONGENITAL; HUMANS; HYDROCEPHALUS; POLYCYSTIC KIDNEY DISEASES; SYNDROME;

EID: 0031726598     PISSN: 03010449     EISSN: None     Source Type: Journal    
DOI: 10.1007/s002470050468     Document Type: Conference Paper

References (4)

1. Cumming W, Ohlsson A, Ali A (1986) Campomelia, cervical lymphocele, polycystic dysplasia, short gut, polysplenia. Am J Med Gen 25: 783-790
2. Urioste M, Arroyo A, Martinez-Frias M (1991) Campomelia, polycystic dysplasia, and cervical lymphoceles in two sibs. Am J Med Gen 41: 475-477
3. Ming JE, McDonald-McGinn DM, Markowitz RI, Ruchelli E, Zackai EH (1997) Heterotaxia in a fetus with campomelia, cervical lymphocele, polysplenia, and multicystic dysplastic kidneys: expanding the phenotype of Cumming syndrome. Am J Med Gen 73: 419-424
4. Taybi H, Lachman RS (1996) Radiology of syndromes, metabolic disorders, and skeletal dysplasias, 4th edn. Mosby, St. Louis