Total: 1 |
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PMID (PMCID) | ||
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3351901 |
MIXED_SAMPLE | Infant |
Further delineation of the G syndrome: a manageable genetic cause of infantile dysphagia. | ||
Wilson GN, Oliver WJ. J Med Genet. 1988;25(3):157-63. |
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The data from index cases support the concept of the G syndrome as a constellation of midline defects, which include hypertelorism or telecanthus (89%), oesophageal dysmotility (69%), laryngotracheal clefts (44%), cleft palate or bifid uvula (34%), heart defects (29%), hypospadias (100% of males), renal or ureteral anomalies (42%), and mental retardation (38%). |