The child of uncertain sex: 17 years of experience
Autor: | Michael J. Thomsett, Abdulmoein E. Al-Agha, Jennifer A. Batch |
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Rok vydání: | 2001 |
Předmět: |
Male
Sex Determination Analysis Pediatrics medicine.medical_specialty Adolescent Databases Factual Gonadal dysgenesis Humans Medicine Congenital adrenal hyperplasia Pseudohermaphroditism Medical diagnosis Child Retrospective Studies Adrenal Hyperplasia Congenital business.industry Medical record Australia Infant Newborn Infant Retrospective cohort study medicine.disease Penoscrotal hypospadias Child Preschool Karyotyping Pediatrics Perinatology and Child Health Etiology Female business |
Zdroj: | Journal of Paediatrics and Child Health. 37:348-351 |
ISSN: | 1440-1754 1034-4810 |
Popis: | Objective: To review the common clinical presentations, investigations and final diagnosis of children presenting with genital ambiguity. Methodology: Retrospective search of the Royal Children's Hospital, Brisbane, Australia, medical records and personal medical database of one of the authors (MJT) between 1982 and 1999. Results: Fifty-one children aged 0.1-;14 (mean 3.9) years were identified. Twenty-two cases had a 46XX karyotype, and commonly presented with an enlarged phallus (77.2%), urogenital sinus (63.6%) and labioscrotal fold(s) (40.9%). Congenital adrenal hyperplasia (CAH) was the most common final diagnosis (72.7%) . Twenty-nine cases of genital ambiguity had a 46XY karyotype and commonly presented with palpable gonad(s) (75.8%), undescended testes (51.7%), penoscrotal hypospadias (51.7%) and a small phallus (41.3%). Androgen insensitivity and gonadal dysgenesis were the commonest final diagnosis both occurring at a frequency of 17.2%. Conclusions: The results emphasize the importance of CAH as the most common diagnosis in 46XX cases presenting with ambiguous genitalia. Those with 46XY had a wider range of diagnoses. Despite thorough investigation, 23.5% had no definite final diagnosis made. |
Databáze: | OpenAIRE |
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