Moebius syndrome and narcolepsy: A case dissertation☆

نویسندگان

  • Lídia Sabaneeff
  • Henrique Mendes Motta
  • Juliana Castro
  • Sergio Tufik
  • Fernando Morgadinho Santos Coelho
چکیده

Moebius syndrome (MS) is a congenital syndrome characterized by unilateral or bilateral aplasia of the VI and VII cranial nerves, with consequent convergent strabismus and bilateral peripheral facial paralysis. This syndrome might be associated with diurnal excessive sleepiness and muscular hypotony, mimetizing in this manner, narcolepsy. The diagnostic criteria for narcolepsy depend on the presence of REM sleep during the day. As with patients with MS we do not have ocular movements due to the VI nerve paralysis, the absence of horizontal ocular movements might make it difficult to confirm narcolepsy in these patients. The common clinical characteristics of these patients are due to a possible impairment of the same structures that are affected in the central nervous system. However, the mechanism by which it occurs remains to be fully understood. Further electrophysiological researches are necessary to better clarify the association of these two diseases. The objective of this dissertation is to describe and discuss a case of Moebius syndrome with diurnal excessive sleepiness as a differential diagnosis for narcolepsy.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Mirror Movements Identified in Patients with Moebius Syndrome

BACKGROUND Moebius syndrome is a rare disorder with minimum clinical criteria of congenital facial weakness in association with impairment in abduction of one or both eyes. Mirror movements are not known to be associated with Moebius syndrome. CASE REPORT We present three patients who meet minimum criteria for a diagnosis of Moebius syndrome and who also display mirror movements. DISCUSSION...

متن کامل

Moebius Syndrome: A Rare Case Report

Moebius syndrome is an extremely rare disorder. Only approximately few hundred cases have been reported in literature. In a nationwide survey reported in 2003, the prevalence of this syndrome was at least 0.002% of births for the years 1996 to 1998. The definition and diagnostic criteria for Moebius syndrome vary among authors. In most studies, it is defined as congenital facial weakness combin...

متن کامل

An unusual case report showing overlapping Features of Poland and Moebius syndrome

[email protected] Phone no. +91 9501544877 Abstract Moebius and Poland syndromes are rare congenital anomalies. Poland syndrome (PS) is characterized by unilateral aplasia/hypoplasia of the breast and pectoralis muscle and ipsilateral deformities in the extremities. However, Moebius-Poland syndrome is rarer than the isolated syndromic conditions. Moebius syndrome is characterized by unilateral...

متن کامل

Cranial Nerve Mischief Masquerading as Food Allergy: Auriculotemporal (frey’s) Syndrome in a Child with Moebius Syndrome

INTRODUCTION T diagnosis of food allergy can be challenging and many conditions can mimic food allergy. It is imperative to differentiate true food allergy from the ‘mimics’ of food allergy, particularly in children eliminating multiple foods from their diet. This case report describes a child with features of Auriculotemporal (Frey’s) syndrome, posing as multiple food allergies. The child was ...

متن کامل

Augmented superior rectus transposition surgery for vertical strabismus in moebius syndrome.

INTRODUCTION Moebius syndrome is a rare disease characterized by unilateral or bilateral congenital nonprogressive facial nerve palsy along with limitation of ocular abductions. Vertical Rectus Transpositions with posterior fixation suture is known to correct abduction deficiencies in case of Moebius syndrome. Traditionally both superior and inferior rectus transposition are done to prevent any...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:

دوره 7  شماره 

صفحات  -

تاریخ انتشار 2014