The choice is D - both A and C
Urbach-Wiethe disease is a rare genetic disorder that can cause calcification of brain tissue in the temporal lobes; this calcification can cause damage to the amygdalae.
<h3>What are the symptoms of Urbach-Wiethe disease?</h3>
The symptoms of the disease vary greatly from individual to individual.
They may include a hoarse voice, lesions and scarring on the skin, easily damaged skin with poor wound healing, dry, wrinkly skin, and beading of the papules around the eyelids.
<h3>What part of the brain does Urbach-Wiethe disease affect?</h3>
(1994, 1995) investigated a patient suffering from Urbach–Wiethe (UW) syndrome, a very rare autosomal recessive disease, which produces bilateral calcifications in the anterior medial temporal lobes, especially of the amygdalae, in 50–75% of cases (Newton et al., 1971; Staut and Naidich, 1998).
Learn more about Urbach-Wiethe disease here:
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Answer:
Explanation: Loss of habitat (destruction) and loss of genetic variation. Another reason could include hunting.
Answer:
mRNA or messenger RNA goes to ribosomes to dictate the genetic information that it contains .
Explanation:
Ribosomes act as work benches during protein biosynthesis.mRNA also called messenger RNA binds with the smaller subunit of ribosome at the time of translation.
The bound subunit of ribosome reads the genetic information as codons containing three concecuetive nucleotides present in mRNA thus helping tRNA to bring the particular amino acid specific for that codon at the A site or attachment site of ribosome.
Thereafter ribosome moves to the next codon to bring another amino acid and so forth.
Thus mRNA helps ribosome to brings the amino acids at the translation site.
