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Inicio Medicina Clínica (English Edition) Partial 3β-hydroxysteroid dehydrogenase type 2 deficiency: Diagnosis of a novel...
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Vol. 146. Issue 2.
Pages 92-93 (January 2016)
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Vol. 146. Issue 2.
Pages 92-93 (January 2016)
Letter to the Editor
DOI: 10.1016/j.medcle.2015.04.005
Partial 3β-hydroxysteroid dehydrogenase type 2 deficiency: Diagnosis of a novel mutation after positive newborn screening for 21-hydroxylase deficiency
Deficiencia parcial de 3β-hidroxiesteroide deshidrogenasa tipo 2: diagnóstico de una nueva mutación tras cribado neonatal positivo de deficiencia de 21-hidroxilasa
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M. Pilar Bahíllo-Curiesesa,
Corresponding author
pilarbahilloc@yahoo.es

Corresponding author.
, Lourdes Loidi Fernández de Trocónizb, Agustín del Cañizo Lópezc, María José Martínez-Sopenaa
a Servicio de Pediatría, Endocrinología Pediátrica, Hospital Clínico Universitario de Valladolid, Valladolid, Spain
b Fundación Pública Galega de Medicina Xenómica, Santiago de Compostela, A Coruña, Spain
c Servicio de Cirugía Pediátrica, Hospital Clínico Universitario de Valladolid, Valladolid, Spain
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