Fogu G, Spano B, Sanna R, Angius A G, Campus P M, Olzai M G, Sanna M G, Balata A, Chiarolini A
Centro di Genetica Clinica dell'Universita di Sassari, Italia.
Pediatr Med Chir. 1991 Jul-Aug;13(4):397-8.
We report a case of Edward's syndrome showing some symptoms infrequently described in trisomy 18. The authors suggest that the phenotypic expression of symptoms rarely observed in the syndrome may be better interpreted as non specific consequence of the chromosomal imbalance, rather than directly related to genes on chromosome 18. A gene dosage effect for the enzyme Peptidase A, whose gene is mapped on chromosome 18, was also observed.
我们报告了一例爱德华兹综合征病例,该病例表现出一些在18三体综合征中很少描述的症状。作者认为,该综合征中很少观察到的症状的表型表达,可能更好地解释为染色体失衡的非特异性后果,而非直接与18号染色体上的基因相关。还观察到一种酶——肽酶A的基因剂量效应,其基因定位于18号染色体上。