Unilateral Peters' anomaly in an infant with 22q11.2 deletion syndrome

Clinical Dysmorphology

Volumn 17, Issue 4, 2008, Pages 289-290

  Erdoǧan, Murat Kadri ^a   Utine, Gülen Eda ^a   Alanay, Yasemin ^a   Aktaş, Dilek ^a  

^a HACETTEPE UNIVERSITY   (Turkey)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CASE REPORT; CHROMOSOME 22Q; CHROMOSOME DELETION; CLINICAL FEATURE; FACE DYSMORPHIA; HUMAN; INFANT; LEUKOKORIA; MALE; MALFORMATION SYNDROME; PETERS ANOMALY; PRIORITY JOURNAL; SYNDROME DELINEATION;

ABNORMALITIES, MULTIPLE; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; EYE ABNORMALITIES; GENETIC DISEASES, INBORN; HUMANS; INFANT; MALE; SYNDROME;

EID: 55349119537     PISSN: 09628827     EISSN: None     Source Type: Journal    
DOI: 10.1097/MCD.0b013e3283079e7c     Document Type: Article

References (5)

1. Casteels I, Devriendt K (2005). Unilateral Peter's anomaly in a patient with DiGeorge syndrome. J Pediatr Ophthalmol Strabismus 42:311-313.
2. Cvekl A, Tamm ER (2004). Anterior eye development and ocular mesenchyme: new insights from mouse models and human diseases. BioEssays 26:374-386.
3. Forbes BJ, Binenbaum G, Edmond JC, DeLarato N, McDonald-McGinn DM, Zackai EH (2007). Ocular findings in the chromosome 22q11.2 deletion syndrome. J Am Assoc Pediatr Ophthalmol Strabismus 11:179-182.
4. Heon E, Barsoum-Homsy M, Cevrette L, Jacob JL, Milot J, Polemeno R, Musarella MA (1992). Peters' anomaly. The spectrum of associated ocular and systemic malformations. Ophthal Paed Genet 13:137-143.
5. Sowden JC (2007). Molecular and developmental mechanisms of anterior segment dysgenesis. Eye 21:1310-1318.