46, XX/47XX, + 14 mosaicism in a liveborn infant. Issue 3 (June 1977)

• Record Type: Journal Article
• Authors: Martin, A O; Ford, M M; Khalil, N T; Turk, K B; Macintyre, M N
• Is Part Of: Journal of medical genetics. Volume 14:Issue 3(1977)
• Page Start: 214
• Page End: 218
• Publication Date: 1977-06
• Subjects: Medical genetics -- Periodicals; 616.042
• DOI: 10.1136/jmg.14.3.214
• Languages: English
• ISSNs: 1468-6244

Abstract

Abstract : A liveborn infant with the complement 46, XX/47, XX, + 14 shared certain features in common with the following previously reported cases: (1) the one previously reported possible case of trisomy 14, (2) cases in which individuals had at least some portion of chromosome No. 14 in triplicate, and (3) cases of atypical D trisomy (Snodgrass category II). The common features include developmental retardation, wide flat nose with bulbous or wide tip, large mouth with turned down corners (some with protruding lips), short neck (some with redundant skin folds), low-set ears, retrognathia, digital anomalies (usually contractions and deviations), palatal anomalies, and cryptorchidism.