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DOI 10.1515/jpem-2014-0497

Медицинская библиотека · Journal of pediatric endocrinology & metabolism : JPEM · 2015

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

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

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Аннотация

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.

Для цитирования: Um Sap Suzanne Ngo, Koki Paul, Dongmo Felicité Nguefack, De Djob Louis, Tedga Annie, Awa Hubert Mbassi, Chelo David, Boula Angeline. Dyshormonogenesis seems to be more frequent in a group of Cameroonian children with congenital hypothyroidism.. Journal of pediatric endocrinology & metabolism : JPEM. 2015. DOI: 10.1515/jpem-2014-0497.

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