PT  - JOURNAL ARTICLE
AU  - L I Al-Gazali
AU  - L Sztriha
AU  - J Punnose
AU  - W Shather
AU  - M Nork
TI  - Absent pituitary gland and hypoplasia of the cerebellar vermis associated with partial ophthalmoplegia and postaxial polydactyly: a variant of orofaciodigital syndrome VI or a new syndrome?
AID  - 10.1136/jmg.36.2.161
DP  - 1999 Feb 01
TA  - Journal of Medical Genetics
PG  - 161--166
VI  - 36
IP  - 2
4099  - http://jmg.bmj.com/content/36/2/161.short
4100  - http://jmg.bmj.com/content/36/2/161.full
SO  - J Med Genet1999 Feb 01; 36
AB  - We report two sibs with features overlapping those of orofaciodigital syndrome type VI (Varadi syndrome). Both presented at birth with oculomotor abnormalities, dysmorphic facial features, and dysgenesis of the cerebellar vermis. There were minimal oral manifestations (high arched palate) in both of them and one had postaxial polydactyly of both hands and one foot. In addition, there was evidence of aplasia of the pituitary gland on MRI scan in both of them with evidence of hypopituitarism. Both responded well to hormone replacement therapy with improvement in their linear growth and mental ability. These cases may represent a new autosomal recessive midline defect syndrome with features overlapping OFDS VI. Alternatively the features in these children could represent variability within OFDS VI.