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Horm Metab Res 2023; 55(08): 528-535
DOI: 10.1055/a-2111-6571
Original Article: Endocrine Care

Assessment of the Degree of Clinical Suspicion of 21-Hydroxylase Deficiency Prior to the Newborn Screening Result

María Sanz Fernández
1   Department of Pediatrics & Pediatric Endocrinology, Hospital General Universitario Gregorio Marañón, Madrid, Spain
,
Marina Mora Sitja
1   Department of Pediatrics & Pediatric Endocrinology, Hospital General Universitario Gregorio Marañón, Madrid, Spain
,
Lucía Carrascón González-Pinto
1   Department of Pediatrics & Pediatric Endocrinology, Hospital General Universitario Gregorio Marañón, Madrid, Spain
,
Estíbaliz López Herce Arteta
1   Department of Pediatrics & Pediatric Endocrinology, Hospital General Universitario Gregorio Marañón, Madrid, Spain
,
Amparo Rodríguez Sánchez
1   Department of Pediatrics & Pediatric Endocrinology, Hospital General Universitario Gregorio Marañón, Madrid, Spain
› Author Affiliations Funding The study was partially supported by Unidad de Investigación Materno Infantil Fundación Familia Alonso (UDIMIFFA).
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Abstract

The aim of the study was to analyze the clinical suspicion and where patients were when they received the positive result of the neonatal screening for CAH 21OHD. The present data derived from a retrospective analysis of a relatively large group of patients with classical CAH 21OHD patients nosed by newborn screening in Madrid, Spain. During the period from 1990 to 2015 of this study 46 children were diagnosed with classical 21OHD [36 with the salt-wasting (SW) form and 10 with simple virilizing (SV)]. In 38 patients, the disease had not been suspected before the neonatal screening result (30 SW and 8 SV). Thirty patients (79%) were at home without suspicion of any disease, as healthy children, 3 patients (8%) were at home pending completion of the study due to clinical suspicion of any disease (ambiguous genitalia, cryptorchidism) and 5 patients (13%) were admitted to the hospital for reasons unrelated to CAH (sepsis, jaundice, hypoglycemia). It is relevant to note that 69.4% of patients (25/36) with SW form were at home with potential risk of adrenal crisis. Six females had been incorrectly labeled as male at birth. The most frequent reason for clinical suspicion was genital ambiguity in women followed by family history of the disease. Neonatal screening provided better results than clinical suspicion. In the majority of patients with 21OHD the diagnosis by screening was anticipated to the clinical suspicion of the disease even in female patients with ambiguous genitalia.

Key words

neonatal screening - congenital adrenal hyperplasia - 21-hydroxylase deficiency - salt-wasting form - simple virilizing form


Publication History

Received: 20 September 2022

Accepted after revision: 16 June 2023

Accepted Manuscript online:
16 June 2023

Article published online:
31 July 2023

© 2023. Thieme. All rights reserved.

Georg Thieme Verlag
Rüdigerstraße 14, 70469 Stuttgart, Germany

 

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