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.

Brachydactyly

Digits that appear disproportionately short compared to the hand/foot. The word brachydactyly is used here to describe a series distinct patterns of shortened digits (brachydactyly types A-E). This is the sense used here.


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PMID (PMCID)
7617402
 MALE Child
Peters'-Plus syndrome: report on an unusual case.
Camera G, Pozzolo S, Carta M, Righi E.
Pathologica. 1994;86(6):673-5.
The patient had Peters' anomaly, slightly arched eyebrows, long eyelashes, a broad nasal tip; malformed and prominent ears, cleft lip and palate, brachydactyly, fingertip pads, severe growth deficiency, and mild mental retardation.
1856836
 MIXED_SAMPLE Infant
Short stature, brachydactyly, and Peters' anomaly (Peters'-plus syndrome): confirmation of autosomal recessive inheritance.
de Almeida JC, Reis DF, Llerena Junior J, Barbosa Neto J, Pontes RL, Middleton S, Telles LF.
J Med Genet. 1991;28(4):277-9.
Short stature, brachydactyly, and Peters' anomaly (Peters'-plus syndrome): confirmation of autosomal recessive inheritance.