Question

Read the article to learn more about the human

Answer 1

Answer:

Down syndrome, Turner syndrome and Klinefelter syndrome.

Explanation:

Down syndrome, Turner syndrome and Klinefelter syndrome are the genetic disorders which are found in chromosome. Down syndrome is a common genetic disorder that occurs when a person has three copies of 21st chromosome. It is also called  trisomy 21. Due to this disorder, delays occur in physical and mental developmental and disabilities of human body parts.

Answer 2

Answer:

1. Chromosome 11 is made of over 130 million base pairs.

2. Approximately how many genes are found on

chromosome 11? 2000

3. autism (neurexin 1), acute intermittent porphyria, albinism, ataxia-telangiectasia, Beckwith–Wiedemann syndrome, Best's disease, beta-ketothiolase deficiency, beta thalassemia.

4.Autism is related to some changes in chromosome 11, although it is characterized as a psychological disorder. It is usually identified in childhood, between 1 and a half years and 3 years, although the initial signs sometimes appear in the first months of life. The disorder affects the child's communication and ability to learn and adapt. Chromosome 11 Duplication Syndrome is a chromosomal alteration that interferes with child development, which may trigger motor, cognitive, language and socialization delays, inability to perform simple motor activities, weight and height deficit, facial dimorphisms and congenital malformations. Jacobsen's syndrome is an inherited disorder caused by the deletion of a specific region of the long arm of chromosome 11, which covers the 11q24.1 band. Patients with this disorder have a phenotype characterized by delayed neuropsychomotor development, craniofacial anomalies, diverse heart defects and blood dyscrasias. Signs and symptoms include: Heart defects; mental delay; difficulty feeding in childhood; attention deficit; hyperactivity; skeletal malformation, among others.

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