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1.
Rev. medica electron ; 40(6): 2120-2139, nov.-dic. 2018.
Article in Spanish | LILACS, CUMED | ID: biblio-978722

ABSTRACT

RESUMEN El síndrome de Moebius es un trastorno polimalformativo no progresivo que se caracteriza por parálisis facial congénita. Se define como una "parálisis congénita de los núcleos de los pares craneales VI y VII, cuyo espectro clínico es variable y se asocia a múltiples malformaciones óseas y musculares. Es poco frecuente y de etiología vascular, genética o multifactorial. El trabajo, basándose en los fundamentos teóricos más actualizados, pretendió describir las manifestaciones clínicas del síndrome de Moebius y su posible etiología, a propósito de un caso. Se trató de un paciente de 11 años de edad, que al nacimiento presentó asimetría facial, desviación de la comisura labial hacia la izquierda, boca semiabierta, lagrimeo constante y pabellón auricular derecho malformado. Por ser una entidad clínica poco conocida, se expuso el presente caso, portador de un síndrome de Moebius incompleto de causa vascular y multifactorial (AU).


ABSTRACT Moebius syndrome is a non-progressive poli-formative disorder characterized by facial congenital paralysis. It is defined as a congenital paralysis of the VI and VII cranial nerves nuclei, the clinical spectrum of which is variable and associated to several bone and muscular malformations. It is few frequent and has vascular, genetic or multifactorial etiology. This work, based on more updated theoretical fundaments, pretended to describe the clinical manifestations of the Moebius syndrome and its possible etiology on the purpose of a case. It is the case of a patient, aged 11 years, who presented facial asymmetry, lips commissure deviation to the left, semi-opened mouth, constant lagrimeo and deformed right auricular pavilion (pabellon auricular). Because it is a little known clinical entity, this case of a patient having an incomplete Moebius syndrome of vascular and multifactorial cause was presented (AU).


Subject(s)
Humans , Male , Child , Ophthalmology , Astigmatism/diagnosis , Congenital Abnormalities , Mobius Syndrome/diagnosis , Facial Paralysis/diagnosis , Hyperopia/diagnosis , Astigmatism/genetics , Physical Therapy Modalities , Mobius Syndrome/complications , Mobius Syndrome/etiology , Mobius Syndrome/genetics , Mobius Syndrome/epidemiology
2.
J Indian Med Assoc ; 1991 Oct; 89(10): 287-9
Article in English | IMSEAR | ID: sea-96160

ABSTRACT

The dermatoglyphic characteristics of subjects with refractive errors when compared with control group revealed significant differences in both qualitative and quantitative parameters. The loops were increased in male myopics; the whorls were increased in male hypermetropics and astigmatics and the arches were decreased in all types of refractive errors in males. However, the whorls were decreased in female hypermetropics only. The mean total ridge count was significantly higher in male astigmatics only. As regards pattern intensity (fingers) no significant difference in the mean value was observed in either sex with any type of refractive errors when compared with those of controls.


Subject(s)
Adolescent , Adult , Astigmatism/genetics , Child , Dermatoglyphics/classification , Female , Humans , Hyperopia/genetics , India , Male , Myopia/genetics , Refractive Errors/genetics
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