Camptodactyly, cleft palate, and club foot. A syndrome showing the autosomal-dominant pattern of inheritance.

Growth hormone deficiency, Wormian bones, dextrocardia, brachycamptodactyly, and other midline defects

“…Camptodactyly is seen in several syndromes, as summarized elsewhere [Welch and Temtamy, 1966;Goodman et al, 1972;Gordon et al, 1969;Poznanski, 19841. Grosse [1974] reported a family with the Rabenhorst syndrome.…”

Camptodactyly: occurrence in two new genetic syndromes and its relationship to other syndromes.

“…Parish et al (1963) Presence of taurinuria in some cases Autosomal dominant 10. Gordon et al (1969) Cleft palate and club foot Autosomal dominant 11. Present report (Family A) Muscular hypoplasia, peculiar facies, skeletal anomalies, and Autosomal recessive ?…”

“…The aetiology of this defect is heterogeneous; it may be either genetic or occur as a sporadic event of unknown cause (Gordon, Davies, and Berman, 1969). It is further known that several independent heritable disorders are associated with camptodactyly (Welch and Temtamy, 1966).…”

Gordon Syndrome: A Case Report

“…[3] He first described the syndrome in a family showing autosomal dominant transmission through three generations. Thereafter no reports appeared till 1979 when Fahed Halal reported a second family with a pattern consistent with autosomal dominant inheritance with reduced penetrance in females through 5 generations.…”