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PubMed:20809772 JSONTXT 10 Projects

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Id Subject Object Predicate Lexical cue
TextSentencer_T1 0-126 Sentence denotes A case report of a patient with Pfeiffer syndrome, an FGRF 2 mutation (Trp290Cys) and unique ocular anterior segment findings.
T1 0-126 Sentence denotes A case report of a patient with Pfeiffer syndrome, an FGRF 2 mutation (Trp290Cys) and unique ocular anterior segment findings.
TextSentencer_T2 127-135 Sentence denotes PURPOSE:
T2 127-135 Sentence denotes PURPOSE:
TextSentencer_T3 136-264 Sentence denotes To report a case of a child with Pfeiffer syndrome, unique ocular anterior segment findings and a mutation in FGFR2 (Trp290Cys).
T3 136-264 Sentence denotes To report a case of a child with Pfeiffer syndrome, unique ocular anterior segment findings and a mutation in FGFR2 (Trp290Cys).
TextSentencer_T4 265-273 Sentence denotes METHODS:
T4 265-273 Sentence denotes METHODS:
TextSentencer_T5 274-286 Sentence denotes Case Report.
T5 274-286 Sentence denotes Case Report.
TextSentencer_T6 287-295 Sentence denotes RESULTS:
T6 287-295 Sentence denotes RESULTS:
TextSentencer_T7 296-476 Sentence denotes We describe a patient with Pfeiffer syndrome with a unique constellation of ocular anterior segment anomalies including microcornea, limbal scleralization, corectopia and glaucoma.
T7 296-476 Sentence denotes We describe a patient with Pfeiffer syndrome with a unique constellation of ocular anterior segment anomalies including microcornea, limbal scleralization, corectopia and glaucoma.
TextSentencer_T8 477-701 Sentence denotes Genomic DNA extraction was heterozygous for a G to T mutation at nucleotide 870 of the fibroblast growth factor receptor 2 gene (FGFR2) which changes tryptophan (TGG) to cysteine (TGT) at amino acid position 290 (Trp290Cys).
T8 477-701 Sentence denotes Genomic DNA extraction was heterozygous for a G to T mutation at nucleotide 870 of the fibroblast growth factor receptor 2 gene (FGFR2) which changes tryptophan (TGG) to cysteine (TGT) at amino acid position 290 (Trp290Cys).
TextSentencer_T9 702-713 Sentence denotes CONCLUSION:
T9 702-713 Sentence denotes CONCLUSION:
TextSentencer_T10 714-940 Sentence denotes This case supports the association between Pfeiffer syndrome and severe ocular anterior segment anomalies, including glaucoma, and underscores the possible role that FGFR2 has in development of the anterior segment of the eye.
T10 714-940 Sentence denotes This case supports the association between Pfeiffer syndrome and severe ocular anterior segment anomalies, including glaucoma, and underscores the possible role that FGFR2 has in development of the anterior segment of the eye.