Distal 10q trisomy associated with bilateral hydronephrosis in infancy

Genetic Counseling

Volumn 14, Issue 3, 2003, Pages 359-362

  Chen, Chin Ping ^a,b   Lin, S P ^a  

^a MACKAY MEMORIAL HOSPITAL   (Taiwan)

^b NATIONAL YANG MING UNIVERSITY   (Taiwan)

Author keywords

Distal 10q trisomy; Hydronephrosis; Infancy; Monosomy 22p

Indexed keywords

ARTICLE; CASE REPORT; CHROMOSOME ANALYSIS; CHROMOSOME DUPLICATION; CLINICAL FEATURE; DOWNWARD PALPEBRAL SLANT; ECHOGRAPHY; ELECTROCARDIOGRAPHY; HEART ATRIUM SEPTUM DEFECT; HUMAN; HYDRONEPHROSIS; HYDROURETER; HYPERTELORISM; KIDNEY FAILURE; LOW SET EAR; MALE; MECONIUM ASPIRATION; MICROGNATHIA; NEWBORN; PARTIAL MONOSOMY; PHYSICAL EXAMINATION; RECIPROCAL CHROMOSOME TRANSLOCATION; RESPIRATORY DISTRESS; TRISOMY; TRISOMY 10;

CHROMOSOMES, HUMAN, PAIR 10; CYTOGENETIC ANALYSIS; GENE DUPLICATION; HUMANS; HYDRONEPHROSIS; INFANT; MALE; TRANSLOCATION, GENETIC; TRISOMY; UROLOGIC DISEASES;

EID: 0141532986     PISSN: 10158146     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (6)

1. CHEN C.-P., SHIH J.-C., LEE C.-C., CHEN L.-F. WANG W., WANG T.-Y.: Prenatal diagnosis of a fetus with distal 10q trisomy. Prenat. Diagn., 1999, 19, 876-878.
2. FRYNS J.P.: Chromosome 10, trisomy 10q2. In: Birth Defects Encyclopedia. M.L. Buyse (ed.). Cambridge, Blackwell Scientific Publications, 1990, 359-360.
3. GARCÍA-HERAS J., MARTIN J.A., WITCHEL S.F., SCACHERI P.: De novo der(X)t(X:10)(q26:q21) with features of distal trisomy 10q: case report of paternal origin identified by late replication with BrdU and the human androgen receptor assay (HAR). J. Med. Genet., 1997, 34, 242-245.
4. MORENO-FUENMAYOR H, ZACKAI E.H., MELLMAN W.J., ARONSON M.: Familial partial trisomy of the long arm of chromosome 10 (q24-26). Pediatrics, 1975, 56, 756-761.
5. PAULI R.M., KIRKPATRICK S.J., MEISNER L.F., MIJANOVICH J.R., SPRITZ R.A.: Neonatal death in cousins with trisomy 10q and monosomy 4p due to a familial translocation. Clin. Genet., 1982, 22, 340-347.
6. YUNIS J.J., SÁNCHEZ O.: A new syndrome resulting from partial trisomy for the distal third of the long arm of chromosome 10. J. Pediatr., 1974, 84, 567-570.