Marshall syndrome

A malformation syndrome that is characterized by facial dysmorphism, severe hypoplasia of the nasal bones and frontal sinuses, ocular involvement, early-onset hearing loss, skeletal and anhidrotic ectodermal anomalies and short stature with spondyloepiphyseal dysplasia and early-onset osteoarthritis.

Glaucoma

Glaucoma refers loss of retinal ganglion cells in a characteristic pattern of optic neuropathy usually associated with increased intraocular pressure.


Total: 2

                      


(per page)
PMID (PMCID)
9489375
MALE Child
[A case of Marshall syndrome with secondary glaucoma due to spontaneous rupture of the lens capsule].
Endo S, Hashimoto Y, Ishida N, Kusano Y, Ohkoshi K, Yamaguchi T.
Nippon Ganka Gakkai Zasshi. 1998;102(1):75-9.
[A case of Marshall syndrome with secondary glaucoma due to spontaneous rupture of the lens capsule].
30650974
MIXED_SAMPLE Infant
Marshall and stickler syndrome in one family.
Tomikova D, Buanyova B, Krasnik V, Gerinec A.
Cesk Slov Oftalmol. 0000;74(3):108-111.
Key words: Marshall syndrome, Stickler syndrome, mid-facial dysmorfism, myopia, glaucoma, cataract.