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lüll The orocraniodigital syndrome of Juberg and Hayward Verloes A; Le Merrer M; Davin JC; Wittamer P; Abrassart C; Bricteux G; Briard MLJ Med Genet 1992[Apr]; 29 (4): 262-5We report three new isolated cases of orocraniodigital syndrome (Juberg-Hayward syndrome). The main clinical features of this unusual birth defect (six patients from three families described so far) are cleft lip/palate, hypertelorism, bowed and upward slanting eyebrows, thumb hypo/aplasia or proximal/distal thumb displacement, luxation of the radial head, elbow restriction, minor vertebral and rib anomalies, and horseshoe kidneys. New features observed in our patients are severe mental impairment (not correlated with the severity of the malformations), anterior anal displacement, and ptosis. Recessive inheritance is likely, but autosomal dominant inheritance cannot yet be totally ruled out; therefore, genetic counselling of parents of an affected child and of affected patients themselves must be cautious.|Adolescent[MESH]|Anal Canal/abnormalities[MESH]|Child[MESH]|Diagnosis, Differential[MESH]|Female[MESH]|Humans[MESH]|Infant[MESH]|Intellectual Disability/genetics[MESH]|Orofaciodigital Syndromes/diagnosis/*genetics[MESH] |