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Most children born with Edwards' syndrome appear weak and fragile, and they are often underweight
Fragile X is a genetic abnormality which is inherited and individuals therefore have the condition from birth, although, depending on the severity of the symptoms it is often undetected until early childhood. The average age of diagnosis is 8 years old. If however, parents are known to be carriers of Fragile X, the child may be given a blood test early on which is used to diagnose fragile x.
males have only one copy of the X chromosome. Males who inherit the full mutation are expected to have mental impairment. A female's normal X chromosome may compensate for her chromosome with the fragile X gene mutation
No. Marfan syndrome is found equally across all ethnicities and genders.
Most of the Klinefelter Syndrome affected persons can lead a life which could be considered as normal. However, they might have certain problems related to sexual organs, (among others), and some, - but not all -, could be infertile. The reason for this is their extra chromosome. Females have XX chromosomes, Males have XY chromosomes, and Klinefelter syndrome affected males have XXY chromosomes. They often are prescribed testosterone therapy. More info could be found on related links.
often have frequent ear and sinus infections. Nearsightedness and lazy eye are also common. Many babies with fragile X syndrome may have trouble with sucking and some experience digestive disorders that cause frequent gagging and vomiting
Down's syndrome is increased with advanced maternal age, which is defined as more than 35 years of age.
Patau syndrome occurs in approximately one in 8,000-12,000 live births in the United States.
Males with Klinefelters, often have lower testosterone & additional breast tissue, weaker muscle tone. Sexual function is usually normal but Low sperm count is also common.
Frey's syndrome may be experienced by up to 90% of patients to some extent and causes perspiration on that side of the face with eating
Some of the conditions that occur more often among children with Down syndrome include: heart defects, vision problems and hearing loss.
two chromosomall diseases that aren't inherited are Downs Syndrome, which is an extra chromosome on the number 21, it occurs in 1 in 650 births, often in women over 35, and Klinefelter's Syndrome, which is the presence of an extra x cromosome, ie XXY, it is a result of nondisjunction during gamete formation.