displasia ectodérmica hipoidrótica

Relato de caso: displasia ectodérmica anidrótica

  • Autores:
  • Douglas Bernal Tiago
  • Lorena Murta Dos Santos
  • Caroline de Souza Silva
  • Palavras-chave:
  • displasia ectodérmica anidrótica
  • displasia ectodérmica hipoidrótica
  • hipertermia em recém-nascidos
  • hipodontia infantil
  • hipotricose infantil
Resumo: INTRODUCTION: Anhydrotic Ectodermal Dysplasia (ASD) is a rare genetic disease, with a sex ratio of 5 men to 1 woman. The typical manifestations are absence of sweat or sebaceous glands, changes in hair, nails and teeth. CASE REPORT: We present the case of a pregnant woman (G3P2C0A0) with a second child clinically affected by the disease and investigation of involvement in the fetus. DISCUSSION: ASD is a rare disease, prenatal care is of paramount importance for early diagnosis, as this way, it is possible to offer targeted treatment of the pathology from birth. Keywords: anhydrotic ectodermal dysplasia, hypohidrotic ectodermal dysplasia, infantile hypodontia, infantile hypotrichosis, hyperthermia in newborns. Expandir Resumo Acessar Texto Completo