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Anales de la Sociedad Mexicana de Oftalmología y Archivos de la Asociación Para Evitar la Ceguera en México

2009, Number 5

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Rev Mex Oftalmol 2009; 83 (5)

Síndrome Möbius-Poland: Presentación de un caso

Villagra-Sanjurjo T, Vizzuett-López IV

Language: Spanish
References: 13
Page: 314-317
PDF size: 130.96 Kb.


ABSTRACT

Introduction: The Möbius-Poland syndrome is a rare entity which is characterized by congenital facial paralysis, paralysis of the sixth cranial nerve, agenesis or hypoplasia of the major pectoral muscle and nipple, besides simbraquidactilia, whose etiology has not been fully understood. Case presentation: 10 year old male patient with major pectoral hypoplasia, limited abduction, adduction and right simbraquidactilia. Conclusions: This case is one of the variants of Möbius-Poland syndrome with a peculiarity of having an exotropia instead of an esotropia. It is imperative that these patients are diagnosed early to reduce the effects through rehabilitation.


REFERENCES

  1. Romero D. Estrabismo. México: Editorial Auroch, 2000. pp.245-248.

  2. Wright K, Spiegel P. Pediatric Ophthalmology and Strabismus.USA: Springer, 2003. pp. 906-907.

  3. Ramos de Souza-Diaz C, Goldchmit M. Further considerations about the ophthalmic features of the Möbius sequence, with data of 28 cases. Arq Bras Oftalmol 2007;70(3):451-457.

  4. David JD. Nature and etiology of the Poland anomaly. N Engl J Med 1972;278:487-489.

  5. Castilla EE, Paz JE, Orioli IM. Pectoralis major muscle defect and Poland complex. Am J Med Genet 1979;4:263-269.

  6. Poland A. Deficiency of the pectoralis muscles. Guy’s Hospital Reports 1941;6:191-193.

  7. Sugarman GI, Stark HH. Möbius syndrome with Poland’s anomaly. J Med Genet 1973;10:192-196.

  8. Ramos A, Martín AJ, Santos J. Parálisis facial en la infancia. Aspectos clínicos, diagnósticos y terapéuticos. An Esp Pediatr 1990;3:253.

  9. Portillo R, Aldave R, Reyes J, Castañeda C, Vera J. Parálisis facial periférica congénita familiar. Anales de la Facultad de Medicina 2001;62(4):295-300.

  10. Verzijl H, van der Zwaag B, Cruysberg J, Padberg G. Möbius syndrome redefined: a syndrome of rhombencephalic maldevelopment. Neurology 2003;61:327-333.

  11. Cammarata-Scalisi F. Espectro clínico y etiológico del síndrome de Möbius. Arch Argent Pediatr 2007;105(5):444-446.

  12. Roig Quilis M. Disgenesia Troncoencefálica: los síndromes de Möbius, Cogan y Pierre Robin en revisión. An Pediatr 2005; 62:346-351.

  13. Czeizel A, Vitez M, Lenz W. Birth prevalence of Poland sequence and proportion of its familial cases. Am J Med Genet 1990;36:521-528.




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