Ohdo syndrome, Say-Barber-Biesecker-Young-Simpson variant: MedlinePlus Genetics (2024)

The Say-Barber-Biesecker-Young-Simpson (SBBYS) variant of Ohdo syndrome is a rare condition characterized by genital abnormalities in males, missing or underdeveloped kneecaps (patellae), intellectual disability, distinctive facial features, and abnormalities affecting other parts of the body.

Males with the SBBYS variant of Ohdo syndrome typically have undescended testes (cryptorchidism). Females with this condition have normal genitalia.

Missing or underdeveloped patellae is the most common skeletal abnormality associated with the SBBYS variant of Ohdo syndrome. Affected individuals also have joint stiffness involving the hips, knees, and ankles that can impair movement. Although joints in the lower body are stiff, joints in the arms and upper body may be unusually loose (lax). Many people with this condition have long thumbs and first (big) toes.

The SBBYS variant of Ohdo syndrome is also associated with delayed development and intellectual disability, which are often severe. Many affected infants have weak muscle tone (hypotonia) that leads to breathing and feeding difficulties.

The SBBYS variant of Ohdo syndrome is characterized by a mask-like, non-expressive face. Additionally, affected individuals may have distinctive facial features such as prominent cheeks, a broad nasal bridge or a nose with a rounded tip, a narrowing of the eye opening (blepharophimosis), droopy eyelids (ptosis), and abnormalities of the tear (lacrimal) glands. About one-third of affected individuals are born with an opening in the roof of the mouth called a cleft palate. The SBBYS variant of Ohdo syndrome can also be associated with heart defects and dental problems.

The SBBYS variant of Ohdo syndrome is caused by mutations in the KAT6B gene. This gene provides instructions for making a type of enzyme called a histone acetyltransferase. These enzymes modify histones, which are structural proteins that attach (bind) to DNA and give chromosomes their shape. By adding a small molecule called an acetyl group to histones, histone acetyltransferases control the activity of certain genes. Little is known about the function of the histone acetyltransferase produced from the KAT6B gene. It appears to regulate genes that are important for early development, including development of the skeleton and nervous system.

The mutations that cause the SBBYS variant of Ohdo syndrome likely prevent the production of functional histone acetyltransferase from one copy of the KAT6B gene in each cell. Studies suggest that the resulting shortage of this enzyme impairs the regulation of various genes during early development. However, it is unclear how these changes lead to the specific features of the condition.

Learn more about the gene associated with Ohdo syndrome, Say-Barber-Biesecker-Young-Simpson variant

• KAT6B

Genetic Testing Information

• Genetic Testing Registry: Blepharophimosis - intellectual disability syndrome, SBBYS type

Genetic and Rare Diseases Information Center

• Blepharophimosis-intellectual disability syndrome

Patient Support and Advocacy Resources

• National Organization for Rare Disorders (NORD)

Catalog of Genes and Diseases from OMIM

• OHDO SYNDROME, SBBYS VARIANT; SBBYSS

Scientific Articles on PubMed

• PubMed

• Campeau PM, Lu JT, Dawson BC, Fokkema IF, Robertson SP, Gibbs RA, Lee BH. TheKAT6B-related disorders genitopatellar syndrome and Ohdo/SBBYS syndrome havedistinct clinical features reflecting distinct molecular mechanisms. Hum Mutat.2012 Nov;33(11):1520-5. doi: 10.1002/humu.22141. Epub 2012 Jul 12. Citation on PubMed or Free article on PubMed Central
• Clayton-Smith J, O'Sullivan J, Daly S, Bhaskar S, Day R, Anderson B, Voss AK,Thomas T, Biesecker LG, Smith P, Fryer A, Chandler KE, Kerr B, Tassabehji M,Lynch SA, Krajewska-Walasek M, McKee S, Smith J, Sweeney E, Mansour S, MohammedS, Donnai D, Black G. Whole-exome-sequencing identifies mutations in histoneacetyltransferase gene KAT6B in individuals with the Say-Barber-Biesecker variantof Ohdo syndrome. Am J Hum Genet. 2011 Nov 11;89(5):675-81. doi:10.1016/j.ajhg.2011.10.008. Citation on PubMed or Free article on PubMed Central
• Day R, Beckett B, Donnai D, Fryer A, Heidenblad M, Howard P, Kerr B, MansourS, Maye U, McKee S, Mohammed S, Sweeney E, Tassabehji M, de Vries BB,Clayton-Smith J. A clinical and genetic study of theSay/Barber/Biesecker/Young-Simpson type of Ohdo syndrome. Clin Genet. 2008Nov;74(5):434-44. doi: 10.1111/j.1399-0004.2008.01087.x. Epub 2008 Sep 16. Citation on PubMed
• Lemire G, Campeau PM, Lee BH. KAT6B Disorders. 2012 Dec 13 [updated2020 Jan 2]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH,Gripp KW, Amemiya A, editors. GeneReviews(R) [Internet]. Seattle (WA):University of Washington, Seattle; 1993-2024. Available fromhttp://www.ncbi.nlm.nih.gov/books/NBK114806/ Citation on PubMed
• Masuno M, Imaizumi K, Okada T, Adachi M, Nishimura G, Ishii T, Tachibana K,Kuroki Y. Young-Simpson syndrome: further delineation of a distinct syndrome withcongenital hypothyroidism, congenital heart defects, facial dysmorphism, andmental retardation. Am J Med Genet. 1999 May 7;84(1):8-11. doi:10.1002/(sici)1096-8628(19990507)84:13.0.co;2-2. Citation on PubMed
• Verloes A, Bremond-Gignac D, Isidor B, David A, Baumann C, Leroy MA, StevensR, Gillerot Y, Heron D, Heron B, Benzacken B, Lacombe D, Brunner H, Bitoun P.Blepharophimosis-mental retardation (BMR) syndromes: A proposed clinicalclassification of the so-called Ohdo syndrome, and delineation of two new BMRsyndromes, one X-linked and one autosomal recessive. Am J Med Genet A. 2006 Jun15;140(12):1285-96. doi: 10.1002/ajmg.a.31270. Citation on PubMed
• White SM, Ades LC, Amor D, Liebelt J, Bankier A, Baker E, Wilson M,Savarirayan R. Two further cases of Ohdo syndrome delineate the phenotypicvariability of the condition. Clin Dysmorphol. 2003 Apr;12(2):109-13. doi:10.1097/00019605-200304000-00007. Citation on PubMed