Peters plus syndrome and absence of kidney: A case report

Cases Journal

Volumn 2, Issue 1, 2009, Pages

  Tuli, Navneet ^a   Kumar, Suresh ^a   Sood, Sunandan ^a  

^a Government Medical College and Hospital   (India)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CASE REPORT; COMPUTER ASSISTED TOMOGRAPHY; DISEASE ASSOCIATION; FEMALE; HUMAN; INFANT; KIDNEY AGENESIS; PETERS ANOMALY; RARE DISEASE;

EID: 77953461332     PISSN: 17571626     EISSN: None     Source Type: Journal    
DOI: 10.1186/1757-1626-2-2     Document Type: Article

References (9)

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2. Hittner HM, Ferrel RE, Antoszyk JH, Kretzler FL: Autosomal dominant anterior dysgenesis with variable expressivity-probable linkage to MNS blood group on chromosome 4. Pediatr Res 1981, 15:56.
3. Townsend WM, Font RL, Zimmerman LE: Congenital corneal leukomas. Histopathological findings in 13 eyes with noncentral defect in Descements membrane. Am J Ophthalmol 1974, 77:400.
4. Saal HM, Arunstein RM, Weinbaum P, Poole AE: Autosoomal recessive Robinow-like syndrome with anterior chamber cleavage anomalies. Am J Med Genet 1988, 30:709-718. (Pubitemid 18237866)
5. Kivlin JD, Fineman RM, Crandall AS, Olson RJ: Peters anomaly as a cause of genetic and nongenetic syndromes. Arch Ophthalmol 1986, 104:61-64.
6. Aubertin G, Weiss MM, Saskia AJ: Peter Plus Syndrome. [http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=peters-plus].
7. Regenbogen LS, Eliahou HE: Diseases Affecting the Eye and the Kidney, Basel, Karger. 1993:261-265
8. Warkany J: Congenital Malformations Notes and Comments Chicago, Year Book Medical Publishers; 1975:490.
9. Dahl E, Koseki H, Balling R: Pax genes and organogenesis. Bioessays 1997, 19:755-765.