We report clinical and behavioural evaluation data in 42 Italian girls with triple X syndrome whose diagnosis was made prenatally between 1998 and 2006 in three Italian centres. At initial evaluation, reproductive and medical histories were collected. Clinical assessment of the child was performed by ...
(45,X) in 1–2% of all female conceptions. In more than 90% of cases, pregnancies are not carried to term. Diverse somatic characteristics are associated with surviving Turner syndrome females, including short stature and cardiovascular abnormalities. In addition, most Turner syndrome females are ...
Triple X syndrome (also called trisomy X syndrome, XXX syndrome, or 47,XXX) is a rare genetic condition where females inherit an extra X chromosome. For some females with triple X syndrome, the third X chromosome can be found in every cell in their body. For others, it is only found ...
INTRODUCTION Triple X syndrome (47,XXX) is not extremely rare, although one might think so, as the majority of cases go undiagnosed.1 The incidence has been established to 1/1000 females, since the earliest case series have been published and confirmed by others.2 Triple X syndrome is a ...
The main clinical and biochemical characteristics of patients with triple X syndrome and the control subjects are presented in Table 1. All of the results from the triple X syndrome patients are reported in Table 2. There was no statistically significant difference in height, weight, BMI, or pub...
However, passivity and delayed expressive language skills are generally noted as characteristics of the syndrome and are very likely to have implications for the child's learning. The extremely passive nature of the child may mean that explicit and direct teaching is required if learning is to ...
Although trisomy X and dysgerminoma are coincidental findings in our case report, women with malignant germ cell tumors and abnormal genitalia should be checked for chromosomal aberrations to exclude anomalies carrying a Y chromosome.关键词: Dysgerminoma Triple‐X syndrome Genetic implications ...
(pneumonia, sleep apnea syndrome, polyposis, allergic rhinitis, atopic dermatitis, conjunctivitis, gastroesophageal reflux, diabetes mellitus, hypertension, anxiety, depression), exacerbations, eosinophil count, chest X-ray, computerized tomography scan, allergy test, GP, nurse and pulmonologist visits, ...
Two studies52,53 (38 patients) included patients with asthma–chronic obstructive pulmonary disease overlap syndrome. Seven trials used a crossover study design (448 patients).47,48,52-56 Six of the 20 trials (9032 patients)43,44,57,58 required patients to have had an asthma exacerbation in...
Due to low success rates and long cycles of traditional drug development, the clinical tendency is to apply omics techniques to reveal patient-level disease characteristics and individualized responses to treatment. However, the heterogeneous form of data and uneven distribution of targets make drug dis...