Molecular Syndromology · 2019 · 41 citations · 36 references
MedicineGeneticsMolecular GeneticsCraniofacial GeneticsGenodermatosesHuman GeneticsCongenital Hand AnomaliesCongenital Limb DeformitiesFoot DeformitiesFoot DisordersGenetic DisordersLimb DevelopmentCongenital Limb MalformationsLimb Development MutationsMolecular Cytogenetic DiagnosisNon-syndromic Limb MalformationsPediatric Limb Anomaly ClassificationSplit Hand Foot MalformationSyndromic Limb MalformationsVariable Expressivity
Split-hand/foot malformation (SHFM) is a genetic limb anomaly disturbing the central rays of the autopod. SHFM is a genetically heterogeneous disorder with variable expressivity inherited as syndromic and nonsyndromic forms. We provide an update of the clinical and molecular aspects of nonsyndromic SHFM. This rare condition is highly complex due to the clinical variability and irregular genetic inheritance observed in the affected individuals. Nonsyndromic SHFM types have been reviewed in terms of major molecular genetic alterations reported to date. This updated overview will assist researchers, scientists, and clinicians in making an appropriate molecular diagnosis, providing an accurate recurrence risk assessment, and developing a management plan.
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Wnt3a-/--like phenotype and limb deficiency in Lef1-/-Tcf1-/- mice
Joan Galcerán, Isabel Fariñas, Michael J. Depew et al. · Genes & Development · 1999 · 463 citations · Full text
Hans van Bokhoven, Ben C.J. Hamel, Mike Bamshad et al. · The American Journal of Human Genetics · 2001 · 378 citations · Full text