Peters anomaly

Peters anomaly (PA) is a congenital corneal opacity disorder characterized by a central corneal leukoma that obstructs the pupil leading to visual loss as well as absence of the posterior corneal stroma and Descemet membrane.

Microcephaly

Head circumference below 2 standard deviations below the mean for age and gender.


Total: 2

                       


(per page)
PMID (PMCID)
16957485
 MALE Infant
Neuhauser syndrome and Peters' anomaly.
Yarar C, Yakut A, Yildirim N, Yildiz B, Basmak H.
Clin Dysmorphol. 2006;15(4):249-51.
We report a 9-month-old boy with major features of Neuhauser syndrome, including megalocornea, mental motor retardation, hypotonia, dysmorphic findings (high-arched palate, broad nasal bridge, epicanthus), who also had additional findings such as Peters' anomaly, microcephaly, undescended testicle, patent ductus arteriosus and atrial septal defects.
11822709
 MALE Infant, Newborn
Possible new syndrome of microcephaly with cortical migration defects, Peters anomaly and multiple intestinal atresias: a multiple vascular disruption syndrome.
Shanske AL, Gurland JE, Mbekeani JN, Bello JA, Campbell D, Kleinhaus S.
Clin Dysmorphol. 2002;11(1):67-9.
Possible new syndrome of microcephaly with cortical migration defects, Peters anomaly and multiple intestinal atresias: a multiple vascular disruption syndrome.