Abstract
We present a family with six children of first cousin parents, in which three present with microcephaly, hypertelorism, down-slanting palpebral fissures, ptosis, a broad nasal tip, a short webbed neck, mental retardation and seizures. Two differential diagnosis, the Noonan and the Baraitser-Winter syndrome are discussed. The possibility of the description of a new MCA/MR syndrome is raised.
Publication types
-
Case Reports
-
Research Support, Non-U.S. Gov't
MeSH terms
-
Abnormalities, Multiple / genetics*
-
Astigmatism / genetics
-
Blepharoptosis / genetics*
-
Brain / abnormalities
-
Child
-
Child, Preschool
-
Consanguinity
-
Face / abnormalities*
-
Female
-
Genes, Recessive
-
Humans
-
Hypertelorism / genetics*
-
Intellectual Disability / genetics*
-
Male
-
Neck / abnormalities
-
Nose / abnormalities
-
Nystagmus, Pathologic / congenital
-
Nystagmus, Pathologic / genetics
-
Pedigree
-
Seizures / genetics
-
Syndrome