2006, Number 4
<< Back Next >>
Anales de Radiología México 2006; 5 (4)
Congenital face paralysis. Report of a case
Barba PSA, Camacho PMA, Ramírez AC, Cano JGZ, Ávila FF
Language: Spanish
References: 14
Page: 337-343
PDF size: 126.65 Kb.
ABSTRACT
Introduction: 14 months-old female Patient referred due to left facial paralysis from the birth, manifested by a deviation of the labial comissure and ptosis palpebral accented with crying. No associate malformations were evident.
Materials and method: Magnetic Resonance of the cranium was carried out , simultaneously with a FIESTA 3D pulse imaging sequence for evaluating VII and VIII cranial pairs to cistern and intra channeled level, showing absence of the facial left nerve from emergency in the recess, showing only vestibulocochlear nerve.
Discussion and conclusion: Facial paralysis causes are of two main types: the traumatic ones and embryonary-pathological ones. The embrionary pathological have been associated to a syndrome called syndrome of Moebius that consists on a congenital facial paralysis that is generally bilateral and less frequent unilateral, not interfering with the inferior half of the face and paralysis of the IV pair. It is commonly associated to other anomalies in limbs, absence of pectoralis major muscle and impairment of other cranial pairs with impossibility of ocular closing. It is concluded that the FIESTA 3D sequence is very useful for the evaluation of the cranial pairs, and of the integrity of the facial nerve.
REFERENCES
Moore, Persaud. Embriología básica 5a. Ed. Philadelphia, Pennsylvania, USA: Mac Graw-Hill Interamericana; 1998, p. 218-63.
Meter MS, Hungh DC. Radiología de cabeza y cuello. 4a. Ed. Vol. 2. Madrid, España; Mosby/Elsevier; 2004, p. 1070-1.
Ruiz JG. Tema 24.2.01 Parálisis Faciales Congénitas y al Nacimiento. http://es.wikipedia.org
Olson WH, Bardin W, Walsh GO, Engel K, Moebius syndrome. Lower motor neuron involment and hypogonadotrophic hypogonadism. Neurology 1970; 20: 1002-8.
Anne L, Pastuszak M, Laninia S, Carlos E, Speck-Martins. Use of misoprostol during pregnacy and Möbius’ Syndrome in infants. The New England Journal of Medicine 1998: 338; 1881-5.
Harriëtte TFMV, Bert van der Zwaag, Johannes RMC, Padberg WG. Möbius syndrome redefined. A syndrome of rhombencephalic maldevelopment. Neurology 2003; 61: 327-33.
Evans PR. Nuclear agenesis. Mobius syndrome: The congenital facial diplegia syndrome. Arch Dis Child 1955; 30: 237-243.
Henderson JL. The congenital facial diplegia síndrome: clincal features, pathology and etiology. A review of sixty one cases. Brain 1939; 62: 381-403.
Harriëtte TFMVerzijl, Valk J, Rob de Vries, Padberg GW. Radiologic evidence for absence of the facial nerve in Möbius syndrome. Neurology 2005; 64: 849-55.
JE Punal, MF Siebert, FB Angueira, AV Lorenzo, Castro-Gago M. Three new patients with congenital unilateral facial nerve palsy due to chromosome 22q11 deletion. New England Journal of Medicine 2001; 16(6): 450-2
Pedraza S, Gámez J, Rovira A, Zamora A. Drive E, Raguer N, Ruscalleda J. MRI findings in Möbius síndrome: Correlation with clinical features. American Academy of Neurology. 2000; 55: 1058-60.
Cattaneo L, Chierici E, Bianchi B, Sesenna E, Pavesi G. The localization of facial motor impairment in sporadic Möbius syndrome. Neurology 2006; 66: 1907-912.
Carr MM, Ross DA, Zuker RM. Cranial nerve defects in congenital facial palsy. The New England Journal of Medicine 1997; 26(2): 80-7.
Goldberg C, DeLorie R, Zuker RM, Manktelow R. The effects of Gracilis Muscle Transplatation on Speech in Children with Moebius Syndrome. The Journal of Craniofacial Surgery. 2003; 14: 687-90