2015, Number 2
Noonan's syndrome. Case Report
Language: Spanish
References: 9
Page: 316-320
PDF size: 216.39 Kb.
ABSTRACT
Noonan's syndrome is a genetic, little-known disease, produced for a mutation in the 12q22 chromosome. Few data on this affection exists in Cuba; since studies with a significant sample have not been conducted that demonstrate the real frequency of the affection. An eight year old patient’s case from Banes, Holguín, is presented, to whom the syndrome through comparative technique was diagnosed, and considering the clinics and radiological characteristics. The consent of parents to do and to divulge this report was taken into account. The interest of this case consists on the low frequency of appearing of Noonan's syndrome, in fact, the first one that has been diagnosed at the municipality.REFERENCES
Quintero Noa JL, García Martínez DA, Hernández Cordero MC, Báez Allende L, Valls Pérez O. Hipoacusia neurosensorial en un síndrome de Noonan y secuencia Poland. Rev Cubana Pediatr [revista en Internet]. 2010 [citado 19 Dic 2014];82(3):[aprox. 9p]. Disponible en: http://scielo.sld.cu/scielo.php?pid=S0034-75312010000300007&script=sci_arttext&tlng=en
Pons Castro L, Méndez Sánchez TJ, Naranjo RM, Arias Díaz A, Soto García M, Silveira Simón M. Síndrome de Noonan. Presentación de dos casos. Rev Cubana Oftalmol [revista en Internet]. 2009 [citado 19 Dic 2014];22(1):[aprox. 7p]. Disponible en: http://scielo.sld.cu/scielo.php?script=sci_arttext&pid=S0864-21762009000100013&lng=es&nrm=iso&tlng=es