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        "resumen" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">El seudohipoaldosteronismo &#40;PHA&#41; tipo I m&#250;ltiple es un s&#237;ndrome de resistencia mineralocorticoide&#44; de herencia autos&#243;mica recesiva&#44; que afecta a t&#250;bulo renal&#44; gl&#225;ndulas salivales y sudor&#237;paras y mucosa del colon&#46;</p> <span class="elsevierStyleSectionTitle">Caso 1</span><p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">Reci&#233;n nacida con hermana que falleci&#243; a los 10 d&#237;as de vida con hiperpotasemia&#46; A los 7 d&#237;as de vida presenta deshidrataci&#243;n&#44; hiponatremia&#44; hiperpotasemia&#44; acidosis metab&#243;lica e hipernatriuria&#46; El diagn&#243;stico se bas&#243; en la presencia de aldosterona en plasma&#44; actividad de renina plasm&#225;tica &#40;ARP&#41; y eliminaci&#243;n de sal en sudor muy elevadas&#46; Precis&#243; rehidrataci&#243;n y tratamiento con sal&#44; bicarbonato&#44; resinas de intercambio i&#243;nico y dieta pobre en potasio&#46; Durante el primer a&#241;o de vida requiri&#243; hospitalizaci&#243;n por descompensaciones repetidas&#46; Tras 7 a&#241;os de evoluci&#243;n&#44; a&#250;n precisa suplementos de sal y bicarbonate y resinas de intercambio i&#243;nico&#46; El desarrollo psicomotor y el crecimiento son adecuados&#46;</p> <span class="elsevierStyleSectionTitle">Caso 2</span><p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">Reci&#233;n nacida de 8 d&#237;as con antecedente de consanguinidad en la familia materna&#46; Al ingreso presenta deshidrataci&#243;n severa con hiponatremia&#44; hiperpotasemia&#44; acidosis metab&#243;lica e hipernatriuria&#44; con aldosterona&#44; ARP y sal en sudor muy elevados&#46; Precisa rehidrataci&#243;n&#44; suplementos de sal y bicarbonato y resinas de intercambio i&#243;nico&#46; Permanece ingresada durante 6 meses por descompensaciones m&#250;ltiples&#44; siendo posible posteriormente control ambulatorio&#46; Al a&#241;o de edad&#44; la curva de peso y el desarrollo psicomotor son adecuados&#46;</p> <span class="elsevierStyleSectionTitle">Conclusiones</span><p id="spar0020" class="elsevierStyleSimplePara elsevierViewall">Se debe sospechar PHA I m&#250;ltiple en reci&#233;n nacidos con s&#237;ndrome pierdesal e hiperpotasemia&#44; sin virilizaci&#243;n&#44; hiperpigmentaci&#243;n ni d&#233;ficit glucocorticoide&#44; que no responde al tratamiento con mineralocorticoides&#46; La labilidad en el primer a&#241;o de vida obliga al ingreso hospitalario prolongado&#46; A edades posteriores es susceptible de control ambulatorio&#46;</p>"
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        "resumen" => "<p id="spar0025" class="elsevierStyleSimplePara elsevierViewall">Multiple type I pseudohypoaldosteronism &#40;PHA-I&#41; is an autosomal recessive condition with multiple target-organ unresponsiveness to aldosterone&#44; manifested early after birth with severe salt-wasting and hyperkalemia&#46;</p> <span class="elsevierStyleSectionTitle">Case 1</span><p id="spar0030" class="elsevierStyleSimplePara elsevierViewall">Female infant born at term after an uneventful pregnancy&#46; One female sibling died in the first week of life with hyperkalemia&#46; The diagnosis of multiple PHA-I resulted from a picture of dehydratation&#44; hyperkalemia and hyponatremia with increased plasma renin activity &#40;PRA&#41;&#44; plasma aldosterone and sweat electrolytes&#46; The treatment consisted of salt and sodium bicarbonate supplements&#44; restricted potassium intake&#44; cation exchange resins and high fluir intale&#46; During first year she was hospitalized for severe salt-losing crises&#46; At 7 years of age&#44; she needs salt and sodium bicarbonate supplements and cation exchange resins&#46; She has a normal growth andneurodevelopment&#46;</p> <span class="elsevierStyleSectionTitle">Case 2</span><p id="spar0035" class="elsevierStyleSimplePara elsevierViewall">Seven-day female newborn with consanguinity in maternal family&#46; Pregnancy and delivery were uncomplicated&#46; On admission she was severely dehydrated with hyponatremia&#44; hyperkalemia&#44; metabolic acidosis and elevated PRA&#44; plasma aldosterone and sweat electrolytes&#46;She remained hospitalized for six months and she was dependent on high amounts of salt and sodium bicarbonate supplements&#44; fluir intake and cation exchange resins&#46; Growth and neurodevelopment are normal&#46;</p> <span class="elsevierStyleSectionTitle">Conclusions</span><p id="spar0040" class="elsevierStyleSimplePara elsevierViewall">Multiple PHA-I may be suspected in a newborn with salt-loss and hyperkalemia without glucocorticoid defect&#46; The frequent episodes of dehydratation during the first year of life require long hospitalization&#46; The improvement with age make posible an ambulatory control after the first year of life&#46;</p>"
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Seudohipoaldosteronismo tipo I múltiple: presentación neonatal y seguimiento
Multiple type i pseudohypoaldosteronism: neonatal management and out-come
M.a Cristina de Frutos Martínez**
Autor para correspondencia
aneumoin@chdo.osakidetza.net

Correspondencia: Unidad de Neumología, Críticos y Urgencias. Servicio de Pediatría. Hospital Aránzazu. P.° Dr. Begiristain, s/n. San Sebastián. Guipúzcoa.
, M.aD. Elorza Martínez, Sofía Salas Hernández, Pilar García Sánchez, Enrique Jaso Cortés, Jesús Pérez-Rodríguez, José Quero Jiménez
Servicio de Neonatología. Hospital Infantil La Paz. Universidad Autónoma de Madrid.
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