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Bartters syndrome?

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Related questions

An individual with Prader-Willi syndrome caused by a deletion (15q11) produced an offspring with Angelman syndrome. Explain the underlying cause of each syndrome in these individuals. Give the sex of the parent with Prader-Willi syndrome syndrome and of the offspring with Angelman syndrome. Most cases of Prader-Willi syndrome (75%) are the result of a deletion, however in 25% of individuals with the syndrome there is no deletion present. Speculate as to the possible cause of Prader-Willi syndrome in the absence of a deletion.

In human beings 45 chromosomes/ single X/XO abnormality causes

(a) Down’s syndrome

(b) Kinefelter’s syndrome

(c) Turner’s syndrome

(d) Edward’s syndrome.

Viable human aneuploids include:
A. trisomy 1, Wittgart's syndrome.
B. trisomy 12, Palau syndrome.
C. trisomy 17, Michael's syndrome.
D. X monosomy, Turner's syndrome.
E. None of the above.

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