Mild phenotypes in a series of patients with opitz GBBB syndrome with MID1 mutations

Joyce So, Vanessa Suckow, Zofia Kijas, Vera Kalscheuer, Bettina Moser, Jennifer Winter, Marieke Baars, Helen Firth, Peter Lunt, Ben Hamel, Peter Meinecke, Claude Moraine, Sylvie Odent, Albert Schinzel, J. J. Van Der Smagt, Koen Devriendt, Beate Albrecht, Gabriele Gillessen-Kaesbach, Ineke Van Der Burgt, Fred PetrijLaurence Faivre, Julie McGaughran, Fiona McKenzie, John M. Opitz, Timothy Cox, Susann Schweiger*

*Corresponding author for this work
51 Citations (Scopus)


Opitz syndrome (OS; MIM 145410 and MIM 300000) is a congenital midline malformation syndrome characterized by hypertelorism, hypospadias, cleft lip/palate, laryngotracheoesophageal (LTE) abnormalities, imperforate anus, developmental delay, and cardiac defects. The X-linked form (XLOS) is caused by mutations in the MID1 gene, which encodes a microtubule-associated RBCC protein. In this study, phenotypic manifestations of patients with and without MID1 mutations were compared to determine genotype-phenotype correlations. We detected 10 novel mutations, 5 in familial cases, 2 in sporadic cases, and 3 in families for whom it was not clear if they were familial or sporadic. The genotype and phenotype was compared for these 10 families, clinically diagnosed OS patients found not to have MID1 mutations, and 4 families in whom we have previously reported MID1 mutations. This combined data set includes clinical and mutation data on 70 patients. The XLOS patients with MID1 mutations were less severely affected than patients with MID1 mutations reported in previous studies, particularly in functionally significant neurologic, LTE, anal, and cardiac abnormalities. Minor anomalies were more prevalent in patients with MID1 mutations compared to those without mutations in this study. Female MID1 mutation carriers had milder phenotypes compared to male MID1 mutation carriers, with the most common manifestation being hypertelorism in both sexes. Most of the anomalies found in the patients of the present study do not correlate with the MID1 mutation type, with the possible exception of LTE malformations. This study demonstrates the wide spectrum of severity and manifestations of OS. It also shows that XLOS patients with MID1 mutations may be less severely affected than indicated in prior reports.

Original languageEnglish
JournalAmerican Journal of Medical Genetics
Volume132 A
Issue number1
Pages (from-to)1-7
Number of pages7
Publication statusPublished - 01.01.2005

Research Areas and Centers

  • Research Area: Medical Genetics


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