par Van Maldergem, Lionel;Gillerot, Yves;Vamos, Eszter ;Toppet, Michèle ;Watillon, Philippe;Van Vliet, Guy
Référence Acta paediatrica, 81, 4, page (365-367)
Publication Publié, 1992
Référence Acta paediatrica, 81, 4, page (365-367)
Publication Publié, 1992
Article révisé par les pairs
Résumé : | A boy presented with ectrodactyly (lobster claw deformity), bilateral cleft lip and palate, semilobar holoprosencephaly and microcephaly, associated with congenital hypogonadotropic hypogonadism and central diabetes insipidus. Other aspects of pituitary function were normal. We suggest that the ectrodactyly‐ectodermal dysplasia‐clefting syndrome can be associated with a variety of hypothalamo‐pituitary dysfunctions, in addition to the already described isolated growth hormone deficiency. Copyright © 1992, Wiley Blackwell. All rights reserved |