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 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 ...
متن کاملKabuki make-up (Niikawa-Kuroki) syndrome: dental and craniofacial findings in a Brazilian child.
This article reports the case of a Brazilian child diagnosed with Kabuki make-up syndrome (KMS), addressing the clinical features observed, with emphasis on the disease-specific oral and craniofacial manifestations. The patient had the distinctive KMS craniofacial appearance, mild delayed mental development, fingers with prominent fingertip pads and visual deficit. The dental findings included ...
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ژورنال
عنوان ژورنال: Haydarpasa Numune Training and Research Hospital Medical Journal
سال: 2017
ISSN: 1300-6363
DOI: 10.14744/hnhj.2017.74745