ESPE Abstracts (2021) 94 P2-438

1HU Araba, Vitoria, Spain; 2Basque Country University, Vitoria, Spain; 3HU Donosti, San Sebastian, Spain; 4HU Basurto, Bilbao, Spain; 5Basque Country University, San Sebastian, Spain


Of the 67 included DSD patients, 33% were HSCs. 68% women and 32% men, with a total concordance between legal sex, current gender and chromosomal sex. Median age: 10.5 years, IQR 8-14. The most frequent clinical form was non-classical (NC) 45.5%, followed by classical with saline loss (CPS) 41%. The distribution of each clinical form according to the karyotype is significant (P = 0.013), the most frequent with XY karyotype is CPS and in NC forms all cases are XX. Median age at the start of the study: 2.5 months, IQR 0.75-42.5. In 68% the diagnostic process began before 12 months of age. According to gender, when comparing the medians, the results are not significant (P = 0.187). On the other hand, there is a higher median age in men with simple virilizing clinical forms (CVS), with 31.5 months. All cases were genetically defined, median age 1 month, IQR 0-5.2; a de novo mutation (I172N) was even identified. The clinical form with the earliest diagnosis was CPS, IQR 0-1.5 months. Detailing the associated pathologies, the following stand out: 12 uro-genital sinuses, 2 vesico-ureteral refluxes, no cases of testicular maldescent or TARTs, 3 ovarian bands, 3 cases of precocious pubarche, one case of acne and 3 hydroelectrolytic decompensations. No metabolic disorders or osteopenia were described. Regarding the treatment, in no case was prenatal treatment offered. 86.3% are under medical treatment, 23% with glucocorticoids in monotherapy. The NC forms are those with the greatest variability with 30% without treatment, 50% glucocorticoids and 20% mineralo-glucocorticoids, significant differences (P = 0.005). Three cases required psycho-psychiatric treatment, one CPS and two NC. It should be noted that the only two patients who required hospital admission and pharmacological treatment of all DSD were two women with CAH, without a diagnosis of gender dysphoria. 16 surgical procedures were performed, 68% for diagnostic purposes and 7 genitoplasties. Median age of genitoplasties: 29 months, IQR 20.5-37. Registering 6 complications. Regarding the surgical result, 1/3 of patients/family declared it excellent and 1/3 acceptable. While 56% were good-excellent according to surgeon / a. Evaluating the specialist teams, all classify endocrinology and surgical teams as good-excellent, as opposed to psychological assistance (55% bad-terrible and 45% good-excellent). ConclusionsThe post-surgical assessment is consistent according to the surgeon and family/patient. Major surgical procedures are scarce, the majority being diagnostic procedures. We advocate for psychological assistance as the main point of improvement.

Volume 94

59th Annual ESPE (ESPE 2021 Online)

Online,
22 Sep 2021 - 26 Sep 2021

European Society for Paediatric Endocrinology 

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