Multiple choice

Match the following:

 
Column - I Column - II
P. Zinsser-Cole-Engman syndrome 1. Rare recessive genetic disorder of skin with poor wound healing
Q. Urbach-Wiethe disease 2. Autosomal dominant disorder caused by mutations in a connexin gene, GJB6/connexin-30
R. Mendes da Costa syndrome 3. Rare progressive congenital disorder with a highly variable phenotype
S. Clouston syndrome 4. Rare genetic lysosomal storage disease, inherited in an X-linked manner
5. Rare autosomal dominant disorder caused by the mutations in genes encoding for connexin channels proteins in the epidermis

  1. P - 3, Q - 1, R - 5, S - 2

  2. P - 5, Q - 1, R - 4, S - 2

  3. P - 3, Q - 4, R - 5, S - 2

  4. P - 2, Q - 3, R - 4, S - 1

  5. P - 1, Q - 4, R - 5, S - 3
Reveal answer Fill a bubble to check yourself
A Correct answer
Explanation

Correct answer. Zinsser-Cole-Engman syndrome is a rare progressive congenital disorder with a highly variable phenotype. Urbach-Wiethe disease is a rare recessive genetic disorder of skin with poor wound healing. Mendes da Costa syndrome is a rare autosomal dominant disorder caused by the mutations in genes encoding for connexin channels proteins in the epidermis. Clouston syndrome is an autosomal dominant disorder caused by mutations in a connexin gene, GJB6/connexin-30.  

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