LATEST 2024 OBESITY MEDICINE BOARD EXAM (ABOM)
EXAM / OBESITY MEDICINE BOARD REAL EXAM
TESTBANK ALL 500 ACTUAL EXAM QUESTIONS AND
WELL ELABORATED ANSWERS (VERIFIED ANSWERS) A
NEW UPDATED VERSION 2024 | GUARANTEED PASS A+
(BRAND NEW!!)
Underweight BMI range - ANSWER: <18.5
Normal range BMI - ANSWER: 18.5-24.9
Overweight BMI - ANSWER: 25-29.9
Obese BMI - ANSWER: over 30
Obese class 1 BMI - ANSWER: 30-34.9
Obese Class 2 BMI Range - ANSWER: 35-39.9
obese class 3 BMI - ANSWER: 40
FTO gene - ANSWER: Fat mass and obesity associated gene region first locus
unequivocally associated with adiposity- higher BMI/total weight (chromosome 16
q12.2)
Only chromosome that does not show obesity loci? - ANSWER: Y chromosome
Most common syndromal cause of obesity? - ANSWER: Prader Willi Syndrome
Autosomal dominant 1/25000
Hypotonia, short stature, hyperphagia
Prader-Willi Syndrome - ANSWER: Most common syndromal cause of obesity
Autosomal dominant
1/25,000
Hypotonia, short stature, hyperphagia
Most common obesity syndrome - ANSWER: MC4R syndrome
1/2000
LEP deficiency - ANSWER: Gene: LEP
Hypogonadism
frequent infections
undetectable serum leptin
, LEPR deficiency - ANSWER: LEPR Gene
Hypogonadism
POMC deficiency - ANSWER: POMC gene
Hypopigmentation
Isolated ACTH deficiency
PCSK1/3 deficiency - ANSWER: PCSK1 gene
Postprandial hypoglycemia
Hypogonadism
Elevated plasma pro insulin
Elevated 32-33 split proinsulin
MC4R deficiency - ANSWER: MC4R gene
Melanocortin 4 receptor
Accelerated growth
Increased final height
BDNf deficiency - ANSWER: BDNF gene
Development delay
Hyperactivity
Impaired memory
Impaired pain sensation
TrkB deficiency - ANSWER: NTRK2 gene
Development delay
Hyperactivity
Impaired memory
Impaired pain sensation
S1M1 deficiency - ANSWER: S1M1 gene
Spectrum of development delay
BBS deficiency - ANSWER: BBS1-16 gene
Polydactyly
Retinal dystrophy
Hypogonadism
Renal abnormalities
Developmental delay
Alstrom Syndrome - ANSWER: ALMS-1 gene
Photophobia
Nystagmus
Visual impairment
Deafness
Severe insulin resistance
Can have high triglycerides
EXAM / OBESITY MEDICINE BOARD REAL EXAM
TESTBANK ALL 500 ACTUAL EXAM QUESTIONS AND
WELL ELABORATED ANSWERS (VERIFIED ANSWERS) A
NEW UPDATED VERSION 2024 | GUARANTEED PASS A+
(BRAND NEW!!)
Underweight BMI range - ANSWER: <18.5
Normal range BMI - ANSWER: 18.5-24.9
Overweight BMI - ANSWER: 25-29.9
Obese BMI - ANSWER: over 30
Obese class 1 BMI - ANSWER: 30-34.9
Obese Class 2 BMI Range - ANSWER: 35-39.9
obese class 3 BMI - ANSWER: 40
FTO gene - ANSWER: Fat mass and obesity associated gene region first locus
unequivocally associated with adiposity- higher BMI/total weight (chromosome 16
q12.2)
Only chromosome that does not show obesity loci? - ANSWER: Y chromosome
Most common syndromal cause of obesity? - ANSWER: Prader Willi Syndrome
Autosomal dominant 1/25000
Hypotonia, short stature, hyperphagia
Prader-Willi Syndrome - ANSWER: Most common syndromal cause of obesity
Autosomal dominant
1/25,000
Hypotonia, short stature, hyperphagia
Most common obesity syndrome - ANSWER: MC4R syndrome
1/2000
LEP deficiency - ANSWER: Gene: LEP
Hypogonadism
frequent infections
undetectable serum leptin
, LEPR deficiency - ANSWER: LEPR Gene
Hypogonadism
POMC deficiency - ANSWER: POMC gene
Hypopigmentation
Isolated ACTH deficiency
PCSK1/3 deficiency - ANSWER: PCSK1 gene
Postprandial hypoglycemia
Hypogonadism
Elevated plasma pro insulin
Elevated 32-33 split proinsulin
MC4R deficiency - ANSWER: MC4R gene
Melanocortin 4 receptor
Accelerated growth
Increased final height
BDNf deficiency - ANSWER: BDNF gene
Development delay
Hyperactivity
Impaired memory
Impaired pain sensation
TrkB deficiency - ANSWER: NTRK2 gene
Development delay
Hyperactivity
Impaired memory
Impaired pain sensation
S1M1 deficiency - ANSWER: S1M1 gene
Spectrum of development delay
BBS deficiency - ANSWER: BBS1-16 gene
Polydactyly
Retinal dystrophy
Hypogonadism
Renal abnormalities
Developmental delay
Alstrom Syndrome - ANSWER: ALMS-1 gene
Photophobia
Nystagmus
Visual impairment
Deafness
Severe insulin resistance
Can have high triglycerides
