Duke University
NCC National Certification Corporation
NCC Registered Nurse Certified in Neonatal Intensive
Care Nursing RNC- NIC Exam
Course Title and Number: NCC Registered Nurse Certified in
Neonatal Intensive Care Nursing RNC-NIC Exam
Exam Title: Board Exam
Exam Date: Exam 2024- 2025
Instructor: [Insert Instructor’s Name]
Student Name: [Insert Student’s Name]
Student ID: [Insert Student ID]
Examination
180 minutes
Instructions:
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2. Answer all questions.
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NCC National Certification
Corporation 2024-2025 NICU Critical Care RNC Nursing
Certification Exam Comprehensive Review Questions
with Correct Answers | 100% Pass Guaranteed | Graded
A+ |
Read All Instructions Carefully and Answer All the
Questions Correctly Good Luck: -
VATER Syndrome also known as VACTERL - Answer>>
V- vertebral defects: 70% usually smaller than normal
vertebrae that may predispose the infant to developing
scoliosis later in life.
A-Anal atresia or imperforate anus: 55% often requires
surgical correction.
C-Cardiovascular defect: 75% Common heart defects
include VSD, ASD, TEF
T-Tracheoesphageal fistula: 70%
E-Esophageal atresia: 70%
R- Renal anomalies: 50% can be severe including
incomplete formation of the kidneys or obstruction of
urine outflow.
L-Limb anomalies:70% Defects include absent or
displaced thumbs, extra digits, fusion of digits, and
forearm defects
In order for infant to be diagnosed must have 3 of 7
abnormalities.
Karyotype - Answer>> A study of the chromosome of
individual. Human Chromosomes are arranged in 23
pairs. Karyotype is a useful test to determine whether
the chromosomes are normal in number and gross
structure. Ex. trisomy 21 has a extra chromosome 21.
sex chromosomes - Answer>> the 23rd pair of
chromosomes that determine a
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person's sex. A male pair XY, a
female pair XX.
Phenotype - Answer>> The observable features and
characteristics of an individual, as determined by both
their chromosomes and their environment.
Genotype - Answer>> genetically coded inheritable
information stored as an DNA. Genotype is responsible
for the characteristics and physical makeup of an
individual.
clinical signs of Turner syndrome - Answer>> Webbed
neck from fetal lymphoedema; after the swelling
resolves, loose folds of skin are still present on neck.
Broad chest with the wide spaced nipples (shield chest)
Swollen hands and feet
short 4th and 5th metacarpals or metatarsals
increased incidence of congenital hip dislocation
increased incidence of coarctation of the aorta and
bicuspid aortic valve.
Cause of Turner Syndrome - Answer>> most common
chromosomal abnormality. Occurs in 1 in 2000 live
female births. Caused by absence of a set of genes that
form a short arm of one of the X chromosomes. Most
pregnancies that have Turner syndrome end in
spontaneous abortion.
Associated findings in Turner Syndrome - Answer>>
Cardiac: coarctation of aorta, aortic valvular stenosis
Renal: Horseshoe kidneys, unilateral renal agenesis
Learning disabilities; normal intelligence
complications/outcome of Turner syndrome -
Answer>> initial care supportive, Correction of
defects, CV surgery/cosmetic surgery, hormone
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replacement estrogen, growth
hormone
Only 1/3 of patients are diagnosed as newborns
remainder in early adolescence: commonly because
primary amenorrhea
Outcome good despite failure of sexual development
Diagnosis of Turner Syndrome - Answer>> Karyotype
testing
Definition of Autosomal Recessive - Answer>> a
genetic mutation is passed from both mother and
father to infant. ex. cystic fibrosis
Symptoms of Cystic Fibrosis - Answer>> very salty-
tasting skin;
persistent coughing, at times with phlegm;
frequent lung infections;
wheezing or shortness of breath;
poor growth/weight gain in spite of a good appetite;
and
frequent greasy, bulky stools or difficulty in bowel
movements.
Cause/outcome of Cystic fibrosis - Answer>> A
defective gene and its protein product cause the body
to produce unusually thick, sticky mucus that:
1.clogs the lungs and leads to life-threatening lung
infections; and
2.obstructs the pancreas and stops natural enzymes
from helping the body break down and absorb food.
Defective gene located on cystic fibrosis
transmembrane conductance regulator(CFTR) gene
located on chromosome 7.
If not treated die by age 5. Median age of survival is
30's.
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