Say Meyer syndrome is a familial syndrome of trigonocephaly, short stature, and motor and mental retardation. Trigonocephaly is a deformity of the skull in which the vault of the skull is sharply angled just in front of the ears, giving the skull a triangular shape. The syndrome is named after Turkish medical geneticist Burhan Say and AmericanphysicianJulia Meyer.
Pena-Shokeir II syndrome is an autosomal recessive disorder.
Opitz trigonocephalysyndrome is characterized by trigonocephaly, upslanting palpebral fissures, hypoplastic nasal root, wide alveolar ridges, anomalous and posteriorly angulated ears, loose skin, heart anomaly, and arthrogryposis (distal).
Smith-Lemli-Opitz syndrome is characterized by microcephaly with a narrow frontal area, slanted or low-set ears, ptosis, anteverted nostrils, cryptorchidism, and hypospadias.
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