Tetralogy of Fallot

Tetralogy of Fallot is a congenital cardiac malformation that consists of an interventricular communication, also known as a ventricular septal defect, obstruction of the right ventricular outflow tract, override of the ventricular septum by the aortic root, and right ventricular hypertrophy.

Hydronephrosis

Severe distention of the kidney with dilation of the renal pelvis and calices.


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PMID (PMCID)
10327246
 MALE Infant, Newborn
Two brothers with varying combinations of severe developmental delay, epilepsy, microcephaly, tetralogy of Fallot and hydronephrosis.
Ryan A, Burn J, Court S, Jackson T, Clayton Smith J, Barwick D.
Clin Dysmorphol. 1999;8(1):15-8.
Two brothers with varying combinations of severe developmental delay, epilepsy, microcephaly, tetralogy of Fallot and hydronephrosis.
837565
 OTHER Infant, Newborn
A case of double trisomy in a liveborn infant: 48, XXY, "13.
Malhes JB, Moore CM, Gershank JJ.
Clin Genet. 1977;11(2):147-50.
Ambigouous genitalia, microcephaly, microphthalmia, hyoptelorism, single choanal opening, low-set ears, simian creases, Tetralogy of Fallot, bilateral hydronephrosis, and absence of the left ureter characterized an infant the died 1 hour postpartum with the karyotype 48,XXY,+13.