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Congenital Harlequin syndrome as an isolated phenomenon: A case report and review of the literature.
Vidal Esteban, A; Natera-de Benito, D; Martínez Sánchez, D; Reche Sainz, A; Rodríguez Díaz, M R; Alfaro Iznaola, C M; de Santos Moreno, M T.
Afiliação
  • Vidal Esteban A; Department of Pediatrics, Hospital Universitario de Fuenlabrada, Madrid, Spain. Electronic address: arantxa_vidal_esteban@hotmail.com.
  • Natera-de Benito D; Department of Pediatrics, Hospital Universitario de Fuenlabrada, Madrid, Spain. Electronic address: daninatera@hotmail.com.
  • Martínez Sánchez D; Department of Dermatology, Hospital Universitario de Fuenlabrada, Madrid, Spain. Electronic address: diego.martinez@salud.madrid.org.
  • Reche Sainz A; Department of Ophtalmology, Hospital Universitario de Fuenlabrada, Madrid, Spain. Electronic address: alberto.reche@salud.madrid.org.
  • Rodríguez Díaz MR; Department of Pediatrics, Hospital Universitario de Fuenlabrada, Madrid, Spain. Electronic address: mariarocio.rodriguez@salud.madrid.org.
  • Alfaro Iznaola CM; Department of Pediatrics, Hospital Universitario de Fuenlabrada, Madrid, Spain. Electronic address: crisalfaroiznaola@gmail.com.
  • de Santos Moreno MT; Department of Pediatrics, Hospital Clínico San Carlos, Madrid, Spain. Electronic address: tsantos.hflr@salud.madrid.org.
Eur J Paediatr Neurol ; 20(3): 426-30, 2016 May.
Article em En | MEDLINE | ID: mdl-26943985
UNLABELLED: Harlequin syndrome (HS) is a rare autonomic disorder due to a hemifacial cutaneous sympathetic denervation. It is characterized by unilateral diminished sweating and flushing of the face even though after heat or prolonged exercise. It is typically acquired. Congenital cases only represent a 6% of all individuals with HS. All congenital HS cases reported so far showed a concomitant Horner syndrome, probably due to a stellate ganglion involvement. HS represents an uncommon autonomic disorder due to a hemifacial cutaneous sympathetic denervation. It is clinically characterized by a dramatic alteration in facial appearance: ipsilateral denervated pale and dry half from the other intact red and moist half. CONCLUSION: We present, to the best of our knowledge, the first case of a patient with a congenital HS as an isolated phenomenon.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças do Sistema Nervoso Autônomo / Doenças Raras / Rubor / Hipo-Hidrose Limite: Humans / Infant / Male Idioma: En Revista: Eur J Paediatr Neurol Assunto da revista: NEUROLOGIA / PEDIATRIA Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças do Sistema Nervoso Autônomo / Doenças Raras / Rubor / Hipo-Hidrose Limite: Humans / Infant / Male Idioma: En Revista: Eur J Paediatr Neurol Assunto da revista: NEUROLOGIA / PEDIATRIA Ano de publicação: 2016 Tipo de documento: Article