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Clinical profile and aetiologies of delayed puberty: a 15 years' experience from a tertiary centre in Sudan.
Galal, Marwa S; Musa, Salwa A; Babiker, Omer O; Hamdan, Hamdan Z; Abdullah, Mohamed A.
Afiliação
  • Galal MS; Department of Paediatrics and Child Health, Faculty of Medicine, Al-Neelain University, Khartoum, Sudan.
  • Musa SA; Department of Paediatrics and Child Health, Faculty of Medicine, Al-Neelain University, Khartoum, Sudan.
  • Babiker OO; Paediatric Endocrinology Unit, Gaafar Ibn Auf Children's Hospital, Khartoum, Sudan.
  • Hamdan HZ; Sudan Childhood Diabetes Centre, Khartoum, Sudan.
  • Abdullah MA; Al-Neelain University, Faculty of Medicine, Khartoum, Sudan.
J Pediatr Endocrinol Metab ; 35(7): 938-945, 2022 Jul 26.
Article em En | MEDLINE | ID: mdl-35671155
OBJECTIVES: Delayed puberty is a common presentation to endocrine clinics, with adult height, sexual capability and fertility being the main concerns for the child and his/her family. Presentation is variable including short stature and/or absence of secondary sexual characteristics. The aetiology can either be constitutional, functional or permanent hypogonadotropic hypogonadism, permanent hypergonadotropic hypogonadism or unclassified. Despite the importance of this subject, there are no publications from Sudan. METHODS: A retrospective hospital-based study. Records of all patients who were seen in the endocrinology unit at Gaffar Ibn Auf Children's Hospital and were diagnosed as having delayed puberty were reviewed and demographic, clinical, and investigations data were obtained. RESULTS: A total of 136 patients were included in this study. Presentation includes short stature in 52.2%, both short stature and delayed puberty in 27.2%, and delayed puberty in 20.6%. The most common aetiologies were permanent hypogonadotropic hypogonadism and functional hypogonadotropic hypogonadism presented in 37.5% and 36% respectively, while constitutional delay of growth and puberty was found in only 14.7%. Type 1 diabetes mellitus (T1DM) was the most frequent chronic illness followed by coeliac disease. Hypergonadotropic hypogonadism was diagnosed in 11.7%, the majority of which were females. CONCLUSIONS: The aetiological pattern reported in this series highlights the role of nutrition and general well-being in pubertal development, as well as the major impact of genetics and consanguinity on disease patterns. Data from African countries are limited and this is the first reported cohort on delayed puberty from Sudan.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Puberdade Tardia / Nanismo / Hipogonadismo / Síndrome de Klinefelter Tipo de estudo: Diagnostic_studies / Etiology_studies / Observational_studies / Risk_factors_studies Limite: Adult / Child / Female / Humans / Male País/Região como assunto: Africa Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Puberdade Tardia / Nanismo / Hipogonadismo / Síndrome de Klinefelter Tipo de estudo: Diagnostic_studies / Etiology_studies / Observational_studies / Risk_factors_studies Limite: Adult / Child / Female / Humans / Male País/Região como assunto: Africa Idioma: En Ano de publicação: 2022 Tipo de documento: Article