Kabuki Syndrome (KS) is a rare genetic disorder first diagnosed in 1981 (Matsumoto & Niikawa, 2003). It\u27s clinical presentation and treatment is unknown by most clinicians the mental health fields. Children with KS present with unique facial characteristics, mental retardation, health problems and socio-emotional delays that are often mistaken for other diagnostic problems. Literature detailing the psychological and psychosocial features of this disorder is scant, and psychotherapeutic approaches have not been described. In this article we present a brief review of Kabuki Syndrome, highlighting its signs and symptoms. Differential diagnoses are identified to aid the clinician in better understanding this unique and relatively unheard of ...
Kabuki syndrome (KS) is a rare syndrome characterized by multiple congenital anomalies and mental re...
Kabuki syndrome (KS) is a rare syndrome characterized by multiple congenital anomalies and mental re...
Kabuki syndrome is a rare disease manifested by several congenital anomalies, often connected with i...
Introduction: Kabuki syndrome is a rare genetic disorder characterized by mental retardation and typ...
The Kabuki (Niikawa-Kuroki) syndrome was reported in 1981 by Niikawa et al. and Kuroki et al. in a t...
The Kabuki (Niikawa-Kuroki) syndrome was reported in 1981 by Niikawa et al. [19] and Kuroki et al. [...
Kabuki syndrome is rare genetic disorder. Patients with this syndrome are phenotypically similar to ...
The characteristics of a 5-years old girl, referred to a multidisciplinary team for cleft lip and pa...
Kabuki syndrome (KS) (Kabuki make-up syndrome, Niikawa-Kuroki syndrome) is a rare genetic disorder f...
Publisher's version (útgefin grein)Kabuki syndrome is a genetic disorder that can affect multiple bo...
Kabuki (Niikawa-Kuroki) syndrome (KS) is a condition of unknown etiology, characterized by a pentad ...
The Kabuki (make-up) syndrome identified in 1981 has been reported in more than three hundred patien...
Background: Kabuki syndrome is a rare genetic condition characterised by pathological changes within...
To access publisher's full text version of this article, please click on the hyperlink in Additional...
The Kabuki syndrome, or Niikawa-Kuroki syndrome, is a clinically recognizable syndrome of unknown et...
Kabuki syndrome (KS) is a rare syndrome characterized by multiple congenital anomalies and mental re...
Kabuki syndrome (KS) is a rare syndrome characterized by multiple congenital anomalies and mental re...
Kabuki syndrome is a rare disease manifested by several congenital anomalies, often connected with i...
Introduction: Kabuki syndrome is a rare genetic disorder characterized by mental retardation and typ...
The Kabuki (Niikawa-Kuroki) syndrome was reported in 1981 by Niikawa et al. and Kuroki et al. in a t...
The Kabuki (Niikawa-Kuroki) syndrome was reported in 1981 by Niikawa et al. [19] and Kuroki et al. [...
Kabuki syndrome is rare genetic disorder. Patients with this syndrome are phenotypically similar to ...
The characteristics of a 5-years old girl, referred to a multidisciplinary team for cleft lip and pa...
Kabuki syndrome (KS) (Kabuki make-up syndrome, Niikawa-Kuroki syndrome) is a rare genetic disorder f...
Publisher's version (útgefin grein)Kabuki syndrome is a genetic disorder that can affect multiple bo...
Kabuki (Niikawa-Kuroki) syndrome (KS) is a condition of unknown etiology, characterized by a pentad ...
The Kabuki (make-up) syndrome identified in 1981 has been reported in more than three hundred patien...
Background: Kabuki syndrome is a rare genetic condition characterised by pathological changes within...
To access publisher's full text version of this article, please click on the hyperlink in Additional...
The Kabuki syndrome, or Niikawa-Kuroki syndrome, is a clinically recognizable syndrome of unknown et...
Kabuki syndrome (KS) is a rare syndrome characterized by multiple congenital anomalies and mental re...
Kabuki syndrome (KS) is a rare syndrome characterized by multiple congenital anomalies and mental re...
Kabuki syndrome is a rare disease manifested by several congenital anomalies, often connected with i...