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Erschienen in: Indian Journal of Pediatrics 2/2021

11.07.2020 | Scientific Letter

Peters-Plus with Anal Atresia and a Novel Frameshift Mutation

verfasst von: Neha Agrawal, Shubha R. Phadke

Erschienen in: Indian Journal of Pediatrics | Ausgabe 2/2021

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Excerpt

To the Editor: Peters-Plus syndrome (OMIM 261540) is a rare multiple malformation syndrome with characteristic eye anomalies including central corneal opacity, thinning of posterior cornea and iridocorneal adhesions. …
Literatur
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Zurück zum Zitat Richards S, Aziz N, Bale S, et al. Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology. Genet Med. 2015;17:405–24.CrossRef Richards S, Aziz N, Bale S, et al. Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology. Genet Med. 2015;17:405–24.CrossRef
2.
Zurück zum Zitat Weh E, Reis LM, Tyler RC, et al. Novel B3GALTL mutations in classic Peters plus syndrome and lack of mutations in a large cohort of patients with similar phenotypes. Clin Genet. 2014;86:142–8.CrossRef Weh E, Reis LM, Tyler RC, et al. Novel B3GALTL mutations in classic Peters plus syndrome and lack of mutations in a large cohort of patients with similar phenotypes. Clin Genet. 2014;86:142–8.CrossRef
Metadaten
Titel
Peters-Plus with Anal Atresia and a Novel Frameshift Mutation
verfasst von
Neha Agrawal
Shubha R. Phadke
Publikationsdatum
11.07.2020
Verlag
Springer India
Erschienen in
Indian Journal of Pediatrics / Ausgabe 2/2021
Print ISSN: 0019-5456
Elektronische ISSN: 0973-7693
DOI
https://doi.org/10.1007/s12098-020-03416-7

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