Pediatric Endocrinology Review MCQs

PART - 5

Abdulmoein Eid Al-Agha, FRCPCH

Professor of Pediatric Endocrinology,
Website: http://aagha.kau.edu.sa
Seven - year old girl, presented to the endocrine clinic because of
short stature, which was reported since birth. She continued to be
shorter than her schoolmates. On examination (photo). Which
one of the following is a diagnostic investigation?

a) Bone age assessment.

b) Skeletal survey.
c) Thyroid function test.
d) Chromosomal analysis.
 Achondroplasia
• Occurs due to sporadic mutations in the majority of cases but can be
inherited as autosomal dominant condition.
• Achondroplasia is the most common form of disproportionate short
stature.
• Generally recognizable intrauterine because of short limbs &
macrocephaly.
• Limb shortening is predominantly in the proximal segment (rhizomelic).
• A trident hand is a description where the hands are short with stubby
fingers, with a separation between the middle and ring fingers.
• Children with achondroplasia have normal intelligence.
• Specialized growth charts have been developed for head circumference,
height.
• They have significant midface hypoplasia, which increases the risk of
obstructive sleep apnea.
• The narrowing of the foramen magnum can cause brainstem compression
with an increased incidence of sudden infant death.
Achondroplasia
Eighteen – months old boy, brought by his parents because of
increasing bowing of his legs (photo). Nutritional history was
unremarkable. He was on vitamin D prophylactic daily dose (400
units) since birth. His limb x-ray (photo). Which one of the following
is most likely diagnosis?

a) Osteodystrophy.
b) Vitamin D resistant rickets.
c) Blount’s disease.
d) Hypophosphatasia.
 Tibia vara (Blount’s disease)
• Is a growth disorder of the tibia that causes tibial bone to
angle inward, resembling a bowleg.
• It is also known as "tibia vara".
• Described by Dr. Walter Blount (1900–1992) “American
pediatric orthopedic surgeon”.
• Blount's disease occurs in young children & adolescents.
• The cause in majority of cases is unknown.
• Sometimes associated with obesity due to the effects of
weight on the growth plate.
• Is progressive disease.
• Severe bowing of the legs “unilateral or bilateral”.
Eight -week-old infant, brought by his mother because of
previous fractures of the left femur & right tibia happened during
labor. Mother noticed some eye change (photo). Plain x-ray of
his lower limb (photo). What is most likely diagnosis?

a) Hypophosphatasia.
b) Osteogenesis imperfecta.
c) Congenital vitamin D deficiency.
d) Hypophosphatemic rickets.
 Osteogenesis imperfecta (OI)
• Characterized by osteoporosis and recurrent fractures “brittle bone
disease.”
• Clinically has many subtypes that vary in both the degree of bone
fragility and features.
• Blue sclera is present in some types(which can be a normal variant
in the neonatal period) and dentinogenesis imperfecta.
• Type II is lethal type and is often identified prenatally by ultrasound.
• Type III is severe but not lethal, and generally the affected children
are born with numerous fractures and bowed limbs.
• Types I & IV less severe but more common forms of OI, and
patients usually have normal stature but may have multiple
fractures in childhood.
• Associated features include easy bruising & joint hypermobility.
Two-year-old boy was referred for further assessment of his
increasingly bow legs. His maternal uncle has rickets. On chest
examination (photo). blood measurements were obtained: calcium
2.37mmol/l, phosphate 0.13mmol/l , alkaline phosphatase 805IU/l,
PTH 1.3pmol/l. Which one of the following statement is true?

a) Nutritional rickets.
b) Vitamin D dependent type 1 rickets.
c) Vitamin D dependent type 2.
d) X- linked hypophosphatemic Rickets.
 X-linked hypophosphatemic Rickets (XLH)
• Hereditary rickets.
• Is associated with PHEX gene mutation.
• The PHEX gene regulates fibroblast growth factor 23 (FGF23).
• FGF 23 normally inhibits renal reabsorption of phosphate into the
bloodstream.
• Serum calcium within normal or slightly below the reference range.
• Serum phosphate low, alkaline phosphatase high, parathyroid
hormone normal.
• Most importantly, urinary loss of phosphate is above the reference
range.
• Treatment with oral phosphate & one alpha or calcitriol.
• If severe bowing, an osteotomy performed to correct the leg
deformity.
• Burosumab (monoclonal antibody) was licensed in 2018 as the first
drug for this condition.
Twelve- year - old obese girl, mother has noticed abnormal
discoloration around her neck (photo). Her blood pressure was
155/ 110 (repeated). On investigations, her fasting glucose was 155
mg/dl, her liver enzymes were elevated and her serum triglyceride
was high. Which one of the following is most likely diagnosis?

a) Type 2 diabetes.
b) Mody diabetes.
c) Type 1 diabetes.
d) Metabolic syndrome.
 Metabolic syndrome in children
• In recent years, greater concern about the presence of obesity &
metabolic syndrome in children and adolescents.
• Since 1995, a number of reports of type 2 diabetes occurring in obese
children.
• In 1988, Reaven described the relationship of insulin resistance to the
development of three associated disorders:
– type 2 diabetes mellitus, hypertension and dyslipidemia (in releation
to increase waist circumference.
Four – day old boy, with birth weight of 4.5 kg, with normal antenatal
& natal histories. He developed seizure because of repeated
hypoglycemic attacks (lowest RBS reading was 32 mg/dl). His general
look (photo). What is the most likely cause of hypoglycemia?

a) Large for gestation age.

b) Infant of diabetic mother.
c) Septicemia.
d) Beckwith-Wiedemann syndrome.
 Beckwith-Wiedemann syndrome (BWS)
• BWS is an overgrowth syndrome.
• Is genetically heterogeneous disorder that involves an
imprinted region of chromosome 11p15.
• Characterized by:
• Antenatal & postnatal overgrowth.
• Macroglossia.
• Hypoglycemia.
• Hemihypertrophy.
• Ear creases or pits
• Abdominal wall defects (omphalocele).
• Increased risk of embryonal tumors (Wilms’tumor &
hepatoblastoma).
• Mental retardation is uncommon and usually related to
early hypoglycemia.
Six- year old girl, brought to the endocrine clinic because mother
has noticed neck swelling. He is otherwise healthy, well developed
child. Neck swelling was not painful but increasing in size with
growth (photo). Which one of the following is the most likely
diagnosis?

a) Enlarged submandibular lymph node.

b) Small cystic hygroma.
c) Thyroglossal cyst.
d) Laryngocele.
 Thyroglossal cyst
• The cyst is painless, soft, round lump in the front of the neck.
• Typically moves, when the child swallows or sticks their tongue out.
• They are often diagnosed in preschool-aged children or during mid-
adolescence.
• During fetal development, thyroid gland is located at the back of
the tongue which naturally migrates down the neck, passing
through the hyoid bone.
• As the thyroid gland descends, it forms a small channel called the
thyroglossal duct.
• This duct usually disappears once the thyroid gland reaches its final
position in the neck.
• Sometimes part of the duct remains and leaves a pocket.
• A thyroglossal cyst will form when fluid collects in this pocket.
• Surgery should involve removing the entire embryologic remnant.
A neonate was born with abnormal looking genitalia (photo).
Chromosomal analysis revealed 46 XX. Which one of the following is
most likely diagnosis?

a) Congenital adrenal hyperplasia.

b) Congenital lipoid adrenal hyperplasia.
c) Congenital adrenal hypoplasia.
d) Isolated clitoromegaly.
 Congenital adrenal hyperplasia (CAH)
• Autosomal recessive disorder.
• The most common enzyme deficiency of congenital adrenal
hyperplasia is 21‐hydroxylase deficiency.
• In the severe form associated with mineralocorticoid &
glucocorticoid deficiencies.
• Affected female neonates, usually born with ambiguous genitalia.
• Affected male neonates, have normal external genitalia and may
present at 2 - 3 weeks of age with weight loss and poor feeding due
to adrenal insufficiency.
• To prevent the morbidity and mortality of congenital adrenal
hyperplasia, newborn screening programs have been implemented.
• Approximately 75% of patients with CAH due to 21-hydroxylase
deficiency have a relative deficiency of mineralocorticoid.
Three weeks old infant, was born at home, brought by his parents
because of abnormal looking genitalia (photo). Mother reported
that one of her brothers is infertile. Chromosomal analysis revealed
46 XY. Serum testosterone and dihydrotestosterone levels were
high. Which one of the following is most likely diagnosis?

a) Complete androgen insensitivity.

b) Partial androgen insensitivity.
c) 5- α- reductase enzyme deficiency.
d) Testicular biosynthesis defect.
 Partial androgen insensitivity syndrome (PAIS)
• The diagnosis is established in an individual with a 46,XY who has:
– under masculinization of external genitalia.
– impaired spermatogenesis (adulthood).
– Normal size & function of both testes.
– evidence of normal or increased synthesis of testosterone and its
normal conversion to dihydrotestosterone.
• AIS represents a spectrum of defects in androgen action and can be
subdivided into three broad phenotypes:
– Complete androgen insensitivity syndrome (CAIS), with typical
female external genitalia.
– Partial androgen insensitivity syndrome (PAIS) with
predominantly female, or predominantly male external genitalia.
– Mild androgen insensitivity syndrome (MAIS) with typical male
external genitalia.
Four -year old boy, wo was diagnosed sine neonatal period with primary adrenal
insufficiency. Sine then, he was on hydrocortisone replacement therapy with good
compliance from his family. Mother has reported that, for the last 6 months, he
started to have on/off seizure accompanied with regression of his motor milestone
development. He was seen by neurologist who has ordered MRI brain (photo).
Which one of the following is important diagnostic investigation you are going to
order?

a) Do serum ACTH & cortisol level.

b) Do 17 hydroxyprogesterone level.
c) Do serum electrolytes.
d) Do Very long chai fatty acid (VLCFA).
 Adrenoleukodystrophy (ALD)
• ALD is one of a group of disorders caused by a defect of
peroxisomes, which are essential for the breakdown of fatty
acids in cells.
• ALD mostly affects boys because the disease-causing mutation is
located on the X chromosome.
• The condition results in accumulation of very-long-chain fatty
acids in nervous system, adrenal gland, and testes.
• There are three major categories of disease:
– Childhood cerebral form -- appears in mid-childhood (at ages
4 to 8 years)
– Adrenomyelopathy -- occurs in men in their 20s or later in
life.
– Impaired adrenal gland function (Addison-like phenotype) .
sixteen- year-old adolescent male, was presented to the clinic
because of severe anorexia and weight loss for the last 3 months.
His back examination (photo). Vital signs were: BP 94/56, HR
105/min. He was dehydrated. His serum glucose random was 55
mg/dl. Which one of the following is important diagnostic
investigation to order?

a) Serum ACTH.
b) Serum cortisol & ACTH.
c) Adrenal ultrasound.
d) Serum Renin & Aldosterone.
 Addison disease
• Acquired primary adrenal insufficiency results from
autoimmune destruction of the adrenal cortex.
• The presenting complaints include: malaise,
weakness, failure to thrive, weight loss, anorexia,
hypoglycemia, salt craving, abdominal pain, vomiting
& hyperpigmentation.
• On examination, the patient may be hypotensive
and frequently has increased pigmentation over the
knuckles, elbows, knees, ankles, and gums.
Nine - month old boy, was brought by his parents due to repeated
attacks of hypocalcemia since birth, with past history of open
heart surgery at neonatal period. His general examination (photo).
Which one of the following investigations is essential to reach the
diagnosis of hypocalcemia?

a) Serum ionized calcium.

b) Serum phosphate.
c) Serum 25- hydroxy vitamin D.
d) Serum Parathyroid hormone.
 DiGeorge syndrome, “22q11.2 deletion syndrome”
• Is caused by deletion of a small segment of chromosome 22.
• The major features include: congenital heart disease, hypocalcemia
due to hypoparathyroidism & defective T‐cell immunity.
• Truncus arteriosus or interrupted aortic arch are common.
• Facial features include: low‐set ears, microstomia, & hypertelorism.
• Embryologic development defects of the third & fourth brachial
arches and their derivatives, which includes the parathyroid glands,
aortic arch, and thymus gland.
• Infants with low T‐cell functions are at risk for common pathogens
including candida and herpes simplex, and opportunistic infections,
such as Pneumocystis carinii.
• The diagnosis can be confirmed by absence of thymus as detected
by chest radiography or by direct inspection during surgery to
correct their congenital heart defect.
GOOD LUCK

End of part- 5