Kabuki Make-up Syndrome – A Case Report with Electromyographic study
نویسندگان
چکیده
منابع مشابه
Oral features in Kabuki make-up Syndrome.
AIM Kabuki make-up Syndrome is so named because of the characteristic facies of the affected patient. The face is similar to a Kabuki actor's mask. The main aim of this report was to describe the oral features in Kabuki Syndrome, focusing on the tooth anomalies. PATIENTS AND METHODS Five subjects with Kabuki Syndrome, identified by the Child Neuropsychiatric Clinic of the University of Sassar...
متن کاملKabuki Make-Up Syndrome with Bilateral Dislocation of the Hip
Aghoutane Elmouhtadi*, MD; Fezzazi Redouane, MD Department of Orthopedic Pediatric Surgery, Medical University Hospital Mohammed VI, Faculty of Medicine and Pharmacy, Marrakech, Morocco Received: Oct 19, 2011; Accepted: Apr 08, 2012; First Online Available: Jan 17, 2013 Kabuki make-up syndrome (KMS) is a rare multiple congenital anomalies/mental retardation syndrome of unknown cause, first desc...
متن کاملKabuki make-up syndrome with unilateral renal agenesis.
Kabuki syndrome is a multiple congenital anomaly/mental retardation syndrome with a diagnosis that is dependent upon clinical findings. Recognition of this entity is based upon unique facial appearance, including long palpebral fissures with everted lower eyelids, arched eyebrows, fleshy-cup-shaped ears and trapezoid philtrum, postnatal growth retardation, and mild to moderate mental retardatio...
متن کاملLatex allergy in a patient with Kabuki syndrome. Case report.
BACKGROUND AND OBJECTIVES The knowledge of anesthesiologists of specific aspects of patients with rare syndromes is a growing need since those patients are increasingly taken to the operating room. The objective of this report was to describe a case of latex allergy in a patient with Kabuki Syndrome, whose aspects have not been completely explained, alerting anesthesiologists for the possibilit...
متن کاملRecurrent Dislocation of the Patella in Kabuki Make-Up Syndrome
Two patients with Kabuki make-up syndrome with bilateral recurrent dislocation of the patella are presented. They had generalized ligamentous laxity and patellofemoral dysplasia. Both developed patellar dislocation in adolescence and required surgery, with medial transfer of the tibial tuberosity associated with vastus medialis plasty (Insall technique). One postoperative complication occurred ...
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ژورنال
عنوان ژورنال: JOURNAL OF CLINICAL AND DIAGNOSTIC RESEARCH
سال: 2014
ISSN: 2249-782X
DOI: 10.7860/jcdr/2014/9804.5122