【佳學(xué)基因檢測】Ohdo綜合征基因解碼、基因檢測

基因解碼導(dǎo)讀：

Ohdo綜合征是英文Ohdo syndrome中文翻譯。男性患者出現(xiàn)生殖器異常，膝蓋缺失或者發(fā)育不良，臉部特征明顯，身體其他部位也有異?，F(xiàn)象。患者常規(guī)智力天賦低下。這一疾病又被稱為楊-辛普森綜合征, SBSS綜合征。

什么樣的人應(yīng)當(dāng)做Ohdo綜合征基因解碼、基因檢測？

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.

Ohdo綜合征綜合征基因解碼

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.

This condition has an autosomal dominant inheritance pattern, which means one copy of the altered gene in each cell is sufficient to cause the disorder. Almost all reported cases have resulted from new mutations in the gene and have occurred in people with no history of the disorder in their family.

Ohdo綜合征的其他名稱

• blepharophimosis and mental retardation syndrome, Say-Barber/Biesecker/Young-Simpson type
• blepharophimosis-intellectual deficit syndrome, Say-Barber/Biesecker/Young-Simpson type
• BMRS SBBYS
• Ohdo syndrome, Say-Barber-Biesecker variant
• Ohdo syndrome, SBBYS variant
• Say-Barber-Biesecker-Young-Simpson syndrome
• Say-Barber-Biesecker-Young-Simpson variant of Ohdo syndrome
• SBBYS variant of Ohdo syndrome
• SBBYSS
• Young-Simpson syndrome

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