Id |
Subject |
Object |
Predicate |
Lexical cue |
TextSentencer_T1 |
0-124 |
Sentence |
denotes |
Primary congenital glaucoma: three case reports on novel mutations and combinations of mutations in the GLC3A (CYP1B1) gene. |
TextSentencer_T2 |
125-133 |
Sentence |
denotes |
PURPOSE: |
TextSentencer_T3 |
134-318 |
Sentence |
denotes |
To describe three patients with congenital glaucoma homozygous and compound heterozygous for different mutations and benign sequence variants in the cytochrome P 450 1B1 (CYP1B1) gene. |
TextSentencer_T4 |
319-327 |
Sentence |
denotes |
METHODS: |
TextSentencer_T5 |
328-513 |
Sentence |
denotes |
All patients were examined by slit-lamp biomicroscopy, gonioscopy, measurement of the cornea and optic disc, ultrasound biometry, and automated static threshold perimetry when possible. |
TextSentencer_T6 |
514-628 |
Sentence |
denotes |
Direct sequence analysis was performed on DNA extracted from peripheral blood from the patients and their parents. |
TextSentencer_T7 |
629-637 |
Sentence |
denotes |
RESULTS: |
TextSentencer_T8 |
638-847 |
Sentence |
denotes |
For patient 1, a newborn boy with buphthalmos and an opaque cornea, a novel homozygous C/T transition in codon 355 (CGA>TGA) led to a predicted nonsense codon Arg355X truncating the protein by 188 amino acids. |
TextSentencer_T9 |
848-951 |
Sentence |
denotes |
For patient 2, a 24-year-old man, a compound heterozygous mutation 1410-1422del/1546-1555dup was found. |
TextSentencer_T10 |
952-1135 |
Sentence |
denotes |
For patient 3, a 34-year-old man, two novel heterozygous missense mutations resulting in an Ala443Gly and a Glu229Lys amino acid exchange and five benign sequence variants were found. |
TextSentencer_T11 |
1136-1147 |
Sentence |
denotes |
CONCLUSION: |
TextSentencer_T12 |
1148-1229 |
Sentence |
denotes |
Our results confirm the crucial role of CYP1B1 mutations for congenital glaucoma. |
T1 |
0-124 |
Sentence |
denotes |
Primary congenital glaucoma: three case reports on novel mutations and combinations of mutations in the GLC3A (CYP1B1) gene. |
T2 |
125-133 |
Sentence |
denotes |
PURPOSE: |
T3 |
134-318 |
Sentence |
denotes |
To describe three patients with congenital glaucoma homozygous and compound heterozygous for different mutations and benign sequence variants in the cytochrome P 450 1B1 (CYP1B1) gene. |
T4 |
319-327 |
Sentence |
denotes |
METHODS: |
T5 |
328-513 |
Sentence |
denotes |
All patients were examined by slit-lamp biomicroscopy, gonioscopy, measurement of the cornea and optic disc, ultrasound biometry, and automated static threshold perimetry when possible. |
T6 |
514-628 |
Sentence |
denotes |
Direct sequence analysis was performed on DNA extracted from peripheral blood from the patients and their parents. |
T7 |
629-637 |
Sentence |
denotes |
RESULTS: |
T8 |
638-847 |
Sentence |
denotes |
For patient 1, a newborn boy with buphthalmos and an opaque cornea, a novel homozygous C/T transition in codon 355 (CGA>TGA) led to a predicted nonsense codon Arg355X truncating the protein by 188 amino acids. |
T9 |
848-951 |
Sentence |
denotes |
For patient 2, a 24-year-old man, a compound heterozygous mutation 1410-1422del/1546-1555dup was found. |
T10 |
952-1135 |
Sentence |
denotes |
For patient 3, a 34-year-old man, two novel heterozygous missense mutations resulting in an Ala443Gly and a Glu229Lys amino acid exchange and five benign sequence variants were found. |
T11 |
1136-1147 |
Sentence |
denotes |
CONCLUSION: |
T12 |
1148-1229 |
Sentence |
denotes |
Our results confirm the crucial role of CYP1B1 mutations for congenital glaucoma. |