Literature DB >> 26030782

Dyshormonogenesis seems to be more frequent in a group of Cameroonian children with congenital hypothyroidism.

Suzanne Ngo Um Sap, Paul Koki, Felicité Nguefack Dongmo, Louis De Djob, Annie Tedga, Hubert Mbassi Awa, David Chelo, Angeline Boula.   

Abstract

Congenital hypothyroidism is a main congenital endocrine disorder, affecting 1 in 4000 births. It is not well described in sub-Saharan countries, and to draw attention to that issue, we decided to describe affected pediatric patients. We retrospectively analyzed the records of eight patients over a period of 6 years. We analyzed clinical sings of hypothyroidism and psychomotor development; hormonal assays and thyroid ultrasound were performed. We included four boys and four girls aged from 3 to 84 months at diagnosis with a median thyroid-stimulating hormone (TSH) level of 156.5 mUI/L. All except one present with a moderate psychomotor delay. Other clinical signs were classical for hypothyroidism. Thyroid ultrasound performed showed a goiter in half of patients, a normal gland in three of them and a hypoplasic gland in the last one, consonant with dyshormonogenesis. We therefore concluded that dyshormonogenesis seems to be more frequent in our context, and this raised the issue of neonatal screening of hypothyroidism in Africa.

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Year:  2015        PMID: 26030782     DOI: 10.1515/jpem-2014-0497

Source DB:  PubMed          Journal:  J Pediatr Endocrinol Metab        ISSN: 0334-018X            Impact factor:   1.634


  1 in total

1.  [Congenital hypothyroidism in Dakar: about 28 cases].

Authors:  Babacar Niang; Amadou Lamine Fall; Idrissa Demba Ba; Younoussa Keita; Indou Dème Ly; Abou Ba; Aliou Thiongane; Aliou Abdoulaye Ndongo; Djibril Boiro; Lamine Thiam; Aissatou Ba; Morgiane Houngbadji; Mouhamed Fattah; Yaye Joor Djeng; Dieynaba Fafa Cissé; Idrissa Basse; Assane Sylla; Papa Moctar Faye; Saliou Diouf; Ousmane Ndiaye; Mamadou Sarr
Journal:  Pan Afr Med J       Date:  2016-09-29
  1 in total

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