Penta X Syndrome is an extremely rare chromosomal disorder that only affects females. While girls normally only have two X chromosomes, girls with Penta X have five X chromosomes. As of 2011, less than 40 cases have been reported.
What is Pentasomy X (Penta X) Syndrome?
What causes Penta X?
Chromosomes are the 46 rod-like structures containing your DNA that are organized into 23 pairs per cell. The 23rd pair are your two sex chromosomes: either two X chromosomes for girls (XX) or one X and one Y chromosome for boys (XY).
During a process called meiosis, chromosome pairs separate and the mother’s egg (her reproductive cell) is normally left with a single X chromosome. However, there may be errors made during this process in which the chromosome pairs fail to separate, resulting in a cell with an extra X chromosome (also called non-disjunction). If the error is made again with both of those X chromosomes, the following cell can end up with four X chromosomes. The fifth X comes from an X-carrying sperm that fertilizes the egg. When this happens, the egg will develop into a baby with five X chromosomes, or Penta X syndrome.
What causes Penta X?
Girls with Penta X Syndrome typically have delayed growth, resulting in short stature and trouble gaining weight. During infancy and childhood, girls with Penta X may exhibit motor delays, moderate to severe intellectual disability, and speech and communication difficulties. Some girls may experience delayed puberty as well.
What can I do to help my child with Penta X?
Early intervention is key in providing the best outcome for girls with Penta X. Parents may find genetic counseling, special education, physical therapy, speech therapy, and other symptom-related services to be beneficial for not only the child, but also their families and/or caretakers.
COMMON PHYSICAL FEATURES
The most common features of girls with Penta X include:
Malformations of the skull and craniofacial region
Wide-spaced eyes with upslanting eyelid folds (palpebral fissures)
A flat nasal bridge
Low-set, malformed ears
A short neck with a low hairline
Small head size (microcephaly)
Thin enamel, abnormally shaped molars, and an opening on the roof of the mouth (cleft palate)
Curved inward (clinodactyly) and permanent flexion (camptodactyly) of the “pinkies” or fifth fingers
Hyperextension of the elbows and fusion of the forearm bones (radioulnar synostosis)
Unusually close knees and increased space between the ankles (genua valga)
Overlapping toes and club foot (metatarsus varus)
Heart and/or kidney defects
Deficient development of the ovaries and uterus
Our X & Y Disorder Research
The Focus Foundation’s efforts are geared toward X & Y Chromosomal Variations including: 47, XXY (Klinefelter syndrome), 47, XYY (Jacob’s syndrome), 47, XXX (Triple X), 48, XXXX (Tetrasomy X), 48, XXXY, and 49, XXXXY. For further information on Klinefelter syndrome, Jacob’s syndrome, and some of the less commonly occurring X and Y disorders, click on the links that follow:
47,XXY (occurs in 1 out of 650 live births)
Only 25% of males with 47,XXY are ever diagnosed during their lifetimes; fewer than 10% of 47,XXY individuals are identified prior to adolescence. This means that millions of affected children remain undiagnosed–often because they are commonly misdiagnosed as simply having speech or motor delays. More than 500,000 people are believed to have 47,XXY disorders in the United States alone, with an equal distribution across all racial and socio-economic groups.
Testosterone replacement has been shown to have a positive impact on brain function through 9 years of age in multiple research studies over the last 20 years. Thus, it is important to consider early hormonal replacement therapy (EHT) for 47,XXY boys who experience decreased testosterone production during critical developmental periods.…READ MORE
47,XYY (occurs in 1 out of 1,000 live births)
At least 85% of those with 47,XYY are never diagnosed. 47,XYY boys consistently present with language-based Learning Disabilities and difficulties with Motor Planning–both issues that are related to the high rate of dyspraxia and dyslexia associated with the disorder. However, 47,XYY boys are commonly misdiagnosed as simply having speech or motor delays.
Boys with 47,XYY typically reach an average height of between 6’3” and 6’5”…READ MORE
47,XXX (occurs in 1 out of 900 live births)
As many as 1 in 900 girls have 47,XXX. Unfortunately, millions of affected girls are undiagnosed. Girls who are prenatally diagnosed and receive early intervention services typically exhibit fewer and less severe cognitive disabilities.
There is an equal distribution of 47,XXX across all racial and socio-economic groups…READ MORE
48,XXYY (occurs in 1 out of 18,000 live male births)
Boys with 48,XXYY consistently exhibit Language-Based Learning Disabilities (LLD) and difficulties with Motor Planning, issues that are related to the high rate of dyslexia associated with the disorder. However, they seem to be stronger in math and such visual-spatial activities as assembling puzzles or remembering directions.
Intellectual disabilities are common in 48,XXYY, with average full-scale IQs in the range of 70-80. Verbal IQs are seen to be significantly lower than performance IQs, due to language-based learning difficulties…READ MORE
48,XXXX (100 cases have been reported)
48,XXXX (also known as Tetrasomy X or Tetra X) is a rare sex chromosome disorder that was first identified in the early 1960s. Since that time, approximately 100 cases have been reported, although less than 50 are described in scientific literature. Due to the scarcity of this female chromosomal variation, it is difficult to define a common phenotypic presentation. A lack of congenital malformations, mild dysmorphology, and varied developmental trajectory suggests that 48,XXXX is largely underdiagnosed…READ MORE
48,XXXY (occurs in 1 in 18,000 to 1 in 40,000 male births)
48,XXXY can result from meiotic or mitotic nondisjunction (errors in chromosomal separation) and is often considered a variant of Klinefelter syndrome (47,XXY). However, boys with 48,XXXY often exhibit a more complicated neurodevelopmental profile than boys with 47,XXY…READ MORE
49,XXXXY (occurs in 1 in 85,000 to 1 in 100,000 live male births)
The first case of 49,XXXXY syndrome was reported in the 1970s, and this chromosomal variation remains one of the rarest sex chromosome disorders. 49,XXXXY results from nondisjunction (errors in chromosomal separation) of the X chromosome occurring during both Meiosis I and Meiosis II…READ MORE
49,XXXXX Pentasomy X (40 females reported since 2011)
Penta X Syndrome is an extremely rare chromosomal disorder that only affects females. While girls normally only have two X chromosomes, girls with Penta X have five X chromosomes. As of 2011, less than 40 cases have been reported.…READ MORE
Klinefelter Syndrome & Other Names You May hear
What You Can Do Now
If you have received a prenatal diagnosis indicating that your child has an X & Y chromosomal variation, or feel that your son or daughter is experiencing developmental delays or developmental dysfunction, the following options are designed to help you take the next step in securing appropriate treatment or an early diagnosis.