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Kabuki syndrome
Classification and external resources
ICD-10 Q89.8
ICD-9 759.89
OMIM 147920
DiseasesDB 32161

Kabuki syndrome, also previously known as Kabuki makeup syndrome, KMS or Niikawa–Kurok Syndrome, is a very rare pediatric congenital disorder of unknown cause with multiple congenital anomalies and mental retardation. It was discovered by two Japanese scientists, Niikawa and Kuroki. It is named Kabuki Syndrome because of the facial resemblance of affected individuals with white Kabuki makeup, a Japanese traditional theatrical form. The name Niikawa-Kuroki Syndrome relates to the two Japanese doctors who first described this syndrome. On the Kabuki Syndrome listserv, children with this syndrome are called Kabuki Kids, or KKs.

Contents

Description

There is a wide range of congenital problems associated with Kabuki syndrome with large differences between affected individuals. Some of the common problems are heart defects (30%), urinary tract anomalies, hearing loss (50%), hypotonia, and postnatal growth deficiency (83%). Other characteristics include skeletal abnormality, joint laxity, short stature, and unusual dermatoglyphic patterns.[1] They often recurrent ear infections in infancy.

In terms of development, mild to moderate intellectual disability (92%) is a common feature. Also, children with Kabuki syndrome often have distinctive behavioural features. For example, 50% are described as unusually sociable, 30% as engaging in only minimal interaction with others, 74% as liking routine and 87% as having a happy disposition. A few have normal intelligence, most of whom have learning differences such as struggling with fine motor, speech skills, and having a good memory.

There is no indication that the life expectancy of individuals with Kabuki syndrome is shortened. Most medical issues are resolved with medical intervention. The fact that there are relatively few adults known with this syndrome is probably related to its recent discovery in 1980 in Japan and around 1990 in Europe and America.

Appearance

The facial appearance of individuals with this syndrome include long eyelids with turning up of the lateral third of the lower eyelid, a broad and depressed nasal tip, large prominent earlobes, and a cleft or high-arched palate.

Other clinical features often include scoliosis, short fifth finger, persistence of fingerpads, and X-ray abnormalities of the vertebrae, hands, and hip joints.

Causes

Inheritance is thought to be autosomal dominant or X-linked recessive; several chromosomal abnormalities have been found, but none of them appear to be specific to Kabuki Syndrome.

Terminology

Several authors have recommended that the term 'make-up' be removed from the designation of this syndrome because some families considered the term objectionable.[2][3]

See also

References

  1. ^ den Biggelaar AM, Kuijpers-Jagtman AM, Bergé SJ, Katsaros C (December 2006). "Kabuki-syndroom, een congenitaal syndroom met multipele anomalieën (Kabuki syndrome, a congenital syndrome with multiple anomalies)" (in Dutch). Nederlands Tijdschrift Voor Tandheelkunde 113 (12): 516–9. PMID 17193989. http://beheer.ntvt.nl/UserFiles/PDF/NV_1206_R08_516.pdf. Retrieved 2009-05-07.  
  2. ^ Hughes HE, Davies SJ (June 1994). "Coarctation of the aorta in Kabuki syndrome". Archives of Disease in Childhood 70 (6): 512–4. doi:10.1136/adc.70.6.512. PMID 8048822.  
  3. ^ Burke LW, Jones MC (January 1995). "Kabuki syndrome: underdiagnosed recognizable pattern in cleft palate patients". The Cleft Palate-craniofacial Journal 32 (1): 77–84. doi:10.1597/1545-1569(1995)032<0077:KSURPI>2.3.CO;2. PMID 7727492.  

External links

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Kabuki syndrome
Classification and external resources
ICD-10 Q89.8
ICD-9 759.89
OMIM 147920
DiseasesDB 32161

Kabuki syndrome, also previously known as Kabuki makeup syndrome, KMS or Niikawa–Kuroki Syndrome, is a pediatric congenital disorder of suspected genetic origin [1][2] with multiple congenital anomalies and mental retardation. It is very rare, affecting roughly one in every 32,000 individuals. It was discovered and described in 1981 by two Japanese groups, lead by the scientists Niikawa and Kuroki[1] (hence the name). It is named Kabuki Syndrome because of the facial resemblance of affected individuals with white Kabuki makeup, a Japanese traditional theatrical form. On the Kabuki Syndrome listserv, children with this syndrome are called Kabuki Kids, or KKs.

Contents

Description

There is a wide range of congenital problems associated with Kabuki syndrome with large differences between affected individuals. Some of the common problems are heart defects (30%), urinary tract anomalies, hearing loss (50%), hypotonia, and postnatal growth deficiency (83%). Other characteristics include skeletal abnormality, joint laxity, short stature, and unusual dermatoglyphic patterns.[2] They often suffer from recurrent ear infections in infancy.

In terms of development, mild to moderate intellectual disability (92%) is a common feature. Also, children with Kabuki syndrome often have distinctive behavioural features. For example, 50% are described as unusually sociable, 30% as engaging in only minimal interaction with others, 74% as liking routine and 87% as having a happy disposition. A few have normal intelligence, most of whom have learning difficulties such as struggling with fine motor, speech skills, and having a good memory.

There is no indication that the life expectancy of individuals with Kabuki syndrome is shortened. Most medical issues are resolved with medical intervention. The fact that there are relatively few adults known with this syndrome is probably related to its recent discovery in 1980 in Japan and around 1990 in Europe and America.

Appearance

The facial appearance of individuals with this syndrome include long eyelids with turning up of the lateral third of the lower eyelid, a broad and depressed nasal tip, large prominent earlobes, and a cleft or high-arched palate.

Other clinical features often include scoliosis, short fifth finger, persistence of fingerpads, and X-ray abnormalities of the vertebrae, hands, and hip joints.

Causes

Inheritance is thought to be autosomal dominant or X-linked recessive; several chromosomal abnormalities have been found, but none of them appear to be specific to Kabuki Syndrome. In August 2010, a study[3][4] found that two thirds of the cases have a loss-of-function mutation in the MLL2 gene, which is coding for a histone methyltransferase; it can participate in epigenetic programming, and is thought to contribute to developmental processes.

Terminology

Several authors have recommended that the term 'make-up' be removed from the designation of this syndrome because some families considered the term objectionable.[5][6]

See also

References

  1. ^ Yoshikazu Kuroki, Yasuyuki Suzuki, Hiroyuki Chyo, Akira Hata, Ichiro Matsui (October 1981). "A new malformation syndrome of long palpebralfissures, large ears, depressed nasal tip, and skeletal anomalies associated with postnatal dwarfism and mental retardation". The Journal of Pediatrics 99 (4): 570–573. doi:10.1016/S0022-3476(81)80256-9. PMID 7277097. http://www.jpeds.com/article/S0022-3476%2881%2980256-9/abstract. 
  2. ^ den Biggelaar AM, Kuijpers-Jagtman AM, Bergé SJ, Katsaros C (December 2006). "Kabuki-syndroom, een congenitaal syndroom met multipele anomalieën (Kabuki syndrome, a congenital syndrome with multiple anomalies)" (in Dutch). Nederlands Tijdschrift Voor Tandheelkunde 113 (12): 516–9. PMID 17193989. http://beheer.ntvt.nl/UserFiles/PDF/NV_1206_R08_516.pdf. Retrieved 2009-05-07. 
  3. ^ Ng SB, Bigham AW, Buckingham KJ, Hannibal MC, McMillin MJ, Gildersleeve HI et al. (2010). [Expression error: Unexpected < operator "Exome sequencing identifies MLL2 mutations as a cause of Kabuki syndrome."]. Nat Genet 42 (9): 790. doi:10.1038/ng.646. PMID 20711175. 
  4. ^ http://www.genomeweb.com/sequencing/exome-sequencing-study-yields-kabuki-syndrome-gene
  5. ^ Hughes HE, Davies SJ (June 1994). [Expression error: Unexpected < operator "Coarctation of the aorta in Kabuki syndrome"]. Archives of Disease in Childhood 70 (6): 512–4. doi:10.1136/adc.70.6.512. PMID 8048822. 
  6. ^ Burke LW, Jones MC (January 1995). [Expression error: Unexpected < operator "Kabuki syndrome: underdiagnosed recognizable pattern in cleft palate patients"]. The Cleft Palate-craniofacial Journal 32 (1): 77–84. doi:10.1597/1545-1569(1995)032<0077:KSURPI>2.3.CO;2. PMID 7727492. 

External links


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