PubMed ID: 8741923
Author(s): Hansen M, Lucarelli MJ, Whiteman DA, Mulliken JB. Treacher Collins syndrome: phenotypic variability in a family including an infant with arhinia and uveal colobomas. Am J Med Genet. 1996 Jan 2;61(1):71-4.
Journal: American Journal Of Medical Genetics, Volume 61, Issue 1, Jan 1996
We report extreme expression of Treacher Collins syndrome in an infant with arhinia, anotia, absent zygomatic bones, hypoplastic mandibular rami, and bilateral coloboma of iris, choroid plexus, and optic nerves. The Treacher Collins phenotype was mildly expressed in the mother and moderately in the sister. The father had no signs and was not ruled out as the father by DNA fingerprinting, thus making homozygosity by descent in the severely affected son very unlikely.