Clinical Genetics · 1997 · 46 citations · 4 references
MedicineGeneticsPediatricsCraniofacial GeneticsHuman GeneticsOcular GeneticsCongenital Hand AnomaliesCongenital Limb DeformitiesGenetic DisordersGenetic SyndromesHand DisordersNeurocutaneous SyndromesAnterior Chamber MorphologyAutosomal Recessive InheritanceDevelopmental Delay Genetics
Male and female cousins, the offspring of consanguineous Turkish parents, have been affected by a hitherto unreported combination of problems comprising moderate to severe psychomotor developmental delay, ocular anterior chamber abnormality, facial dysmorphisms (broad, bossed forehead, late-closing fontanelle, telecanthus, downslanting palpebral fissures, posteriorly rotated ears, downturned angles of mouth), arachnodactyly and distal arthrogryposis with severely adducted thumbs and club feet. This striking phenotype has some similarities with the multiple pterygium syndrome (Escobar syndrome), but it most likely represents a distinct condition caused by an autosomal recessive gene defect.
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Jan Blancato · Reproductive Toxicology · 1993 · 455 citations
Anna Rajab, Michael Quinn Patton · International Journal of Cardiology · 1994 · 68 citations
Pieter Tamminga, F.G.I. Jennekens, P. G. Barth et al. · European Journal of Pediatrics · 1985 · 18 citations
Medicine, Ophthalmology, Pediatrics +16