Patau syndrome, also known as trisomy 13, is an autosomal genetic disorder caused by the presence of an extra copy of chromosome 13. It is not sex-linked, as it affects chromosomes that are not related to sex determination. This condition can lead to various physical and intellectual disabilities, and it typically results from nondisjunction during cell division.
These are called fatal genetic mutations. Same examples are: Tay-Sachs disease, Neimann-Pick disease, Trisomy 18 and Trisomy 13 are "Edwards Syndrome" and "Patau Syndrome," respectively and Cystic fibrosis
Patau syndrome was first described by Dr. Klaus Patau in 1960.
Neither. Patau syndrome isn't gender-linked. In fact, the majority of the time it isn't even inherited directly from the parents. Patau syndrome is the event where an individual has an extra copy of the 13th chromosome. It most often occurs because of random error in meiosis.
Klaus Patau was born in 1908.
Klaus Patau died in 1975.
nondisjunction
Patau is pronounced as "pa-tow," with the emphasis on the first syllable "pa."
Named for Dr. Klaus Patau, who reported the syndrome in 1960. It is sometimes called Bartholin-Patau syndrome, named in part for Thomas Bartholin, who described an infant with the syndrome in 1656.
Patau's Syndrome Trisomy 13 Syndrome Trisomy D Syndrome Trisomie 13 Trisomee Trisome Trisomic Chromosomal Abnormalities, Chromosome Anomalies, Disorder Fetal Aneuploidy
Feeding difficulties; constipation; reflux disease; slow growth rates; scoliosis; irritability; sunlight sensitivity; low muscle tone; high blood pressure; sinus, urinary tract, ear and eye infections.
in Patau there is an extra chromosome in chromosome 13, in Edwars it the extra chromosome is in chromosome 18
I have it ;)