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Pitt–Hopkins Syndrome and Differential Diagnosis: A Molecular and Clinical Challenge

Pitt–Hopkins syndrome is an emerging neurodevelopmental disorder caused by haploinsufficiency of the TCF4 gene on chromosome 18q21. It is characterized by severe intellectual disability, seizures, microcephaly, constipation and a distinctive facial gestalt. Although the overlapping phenotype of micr...

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Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:J Pediatr Genet
Prif Awduron: Marangi, Giuseppe, Zollino, Marcella
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Georg Thieme Verlag KG 2015
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC4918722/
https://ncbi.nlm.nih.gov/pubmed/27617128
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1055/s-0035-1564570
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