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{{WBRQuestion
{{WBRQuestion
|QuestionAuthor={{Rim}}
|QuestionAuthor= {{Rim}} (Reviewed by  {{YD}})
|ExamType=USMLE Step 1
|ExamType=USMLE Step 1
|MainCategory=Biochemistry, Genetics
|MainCategory=Biochemistry, Genetics
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|MainCategory=Biochemistry, Genetics
|MainCategory=Biochemistry, Genetics
|SubCategory=Renal
|SubCategory=Renal
|MainCategory=Biochemistry, Genetics
|MainCategory=Biochemistry, Genetics
|MainCategory=Biochemistry, Genetics
|MainCategory=Biochemistry, Genetics
|MainCategory=Biochemistry, Genetics
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|MainCategory=Biochemistry, Genetics
|MainCategory=Biochemistry, Genetics
|SubCategory=Renal
|SubCategory=Renal
|Prompt=A 27 year old male presents to the emergency department for severe left flank pain radiating to the groin and associated with hematuria. The pain suddenly started one hour ago and is severe and stabbing in nature. The patient reports that this is not the first time such pain crises happens to him.  According to the patient, previous laboratory exams constantly revealed hexagonal stones in all the previous episodes.  He was informed that the cause of his recurrent kidney stones is a genetic disease in the amino acid transporters in the kidneys. If the patient had a kid with a woman not carrying the disease, what is the percentage his kid will also have the disease?
|Prompt=A 27-year-old man presents to the emergency department with severe left flank pain for the past 3 hours. He states the pain is a sharp, stabbing sensation that radiates to his left groin. Upon further questioning, the patient recalls that he has had similar episodes in the past. Physical examination is remarkable for left costovertebral angle tenderness. Urinalysis demonstrates hematuria and hexagonal-shaped crystals. Following further investigation, the physician explains to the patient that his condition is caused by a genetic disorder characterized by a mutation in an amino acid transporters in the kidneys. If genetic testing reveals the patient's wife does not carry a similar mutation, what is the percentage that this couple's child will have the disease?
|Explanation=The patient presents with recurrent [[kidney stone]]s. The [[urinalysis]] repeatedly reveals hexagonal crystal in all previous episodes, consistent with cystine stone which occurs in patients with [[cystinuria]]. Cystinuria is autosomal recessive disease characterized by abnormal transporters in the kidneys for cysteine and other positively charged amino acids such as [[ornithine]], [[lysine]] and [[arginine]] leading to impaired absorption of these amino acids. Patients with cystinuria are predisposed to cystine stones (cystine is formed of two cysteine linked by disulfide bond).  The treatment of [[cystine]] stones is good hydration and urine alkalinization.
|Explanation=The features of the patient's pain (location, radiation, and severity) and findings on physical examination (costovertebral angle tenderness), and urinalysis (hematuria and hexagonal-shaped crystals) are all consistent with the diagnosis of kidney stones (nephrolithiasis). In addition, the patient's recurrent presentation is concerning and warrants further investigation for an underlying etiology of his condition. Cystinuria is an autosomal recessive genetic disease characterized by reduced renal reabsorption of positively charged amino acids. It is caused by the presence of abnormal transporters in the kidneys for [[cysteine]], [[ornithine]], [[lysine]], and [[arginine]]. Cystinuria results in impaired renal reabsorption and excessive excretion of these amino acids, and patients with cystinuria are predisposed to the development of recurrent cystine stones, which often manifest with hexagonal-shaped crystals on urinalysis. Given the autosomal recessive pattern of inheritance, the patient must have 2 copies of the mutant allele. Given that the mother is not a carrier of the mutant allele, There is a 100% chance that a child may be a silent carrier of the mutation, but a 0% chance that the disease will manifest phenotypically.  
Cystinuria is autosomal recessive; therefore, there is 100% risk that the patient will transmit one allele to his kid. However, since the mother is not a carrier, the kid will only have one mutated allele and consequently will not manifest the disease.
 
'''Educational objective:'''
Cystinuria is an autosomal recessive disease characterized by abnormal reabsorption of cysteine, ornithine, lysine and ornithine (mnemonic: cola) in the proximal convoluted tubules of the kidneys.
 
'''Reference:''' First aid for USMLE step 1, 2013. Page 109.
|AnswerA=0%
|AnswerA=0%
|AnswerAExp=Cystinuria is autosomal recessive; therefore, there is 100% risk that the patient will transmit one allele to his kid. However, since the mother is not a carrier, the kid will only have one mutated allele and consequently will not manifest the disease. Therefore, the patient has 0% risk of having cystinuria.
|AnswerAExp=[[Cystinuria]] is an [[autosomal recessive]] disease. As the mother is not a carrier of the mutant allele (has 2 wild-type alleles), the couple's child would have had 0% chance of developing cystinuria and 100% chance of carrying a mutant allele.
|AnswerB=25%
|AnswerB=25%
|AnswerBExp=Cystinuria is autosomal recessive; therefore, there is 100% risk that the patient will transmit one allele to his kid.  However, since the mother is not a carrier, the kid will only have one mutated allele and consequently will not manifest the disease. Therefore, the patient has 0% risk of having cystinuria.
|AnswerBExp=Had both the child's father and mother been carriers of the mutant allele, they would not have manifested the disease themselves, and their child would have had a 25% chance of developing cystinuria.
|AnswerC=50%
|AnswerC=50%
|AnswerCExp=Cystinuria is autosomal recessive; therefore, there is 100% risk that the patient will transmit one allele to his kid. However, since the mother is not a carrier, the kid will only have one mutated allele and consequently will not manifest the disease. Therefore, the patient has 0% risk of having cystinuria.
|AnswerCExp=Cystinuria is inherited in an autosomal recessive pattern. Patients who manifest the disease have 2 mutant alleles, while carriers of the mutation have only 1 mutant allele. The offspring of an individual with the disease and an individual who carries the allele has a 50% chance of developing the disease.
|AnswerD=75%
|AnswerD=75%
|AnswerDExp=Cystinuria is autosomal recessive; therefore, there is 100% risk that the patient will transmit one allele to his kid. However, since the mother is not a carrier, the kid will only have one mutated allele and consequently will not manifest the disease. Therefore, the patient has 0% risk of having cystinuria.
|AnswerDExp=Cystinuria is inherited in an autosomal recessive pattern. The couple's child has a 0% chance of developing cystinuria.
|AnswerE=100%
|AnswerE=100%
|AnswerEExp=Cystinuria is autosomal recessive; therefore, there is 100% risk that the patient will transmit one allele to his kid. However, since the mother is not a carrier, the kid will only have one mutated allele and consequently will not manifest the disease. Therefore, the patient has 0% risk of having cystinuria.
|AnswerEExp=An example of a 100% chance of a child developing cystinuria is when both parents have fully manifest disease (both carry 2 mutant alleles). In that case all offspring would have the disease too.
|EducationalObjectives=Cystinuria is inherited in an autosomal recessive pattern. Patients who manifest the disease have 2 mutant alleles, while carriers of the mutation have only 1 mutant allele.
|References=First Aid 2014 page 111
|RightAnswer=A
|RightAnswer=A
|WBRKeyword=Cystinuria, cystine, Cysteine,
|WBRKeyword=Cystinuria, Cysteine, Cystine stone, Kidney stone, Nephrolithiasis, Autosomal recessive, Allele, Mutant, Hematuria, Flank pain
|Approved=No
|Approved=Yes
}}
}}

Latest revision as of 02:16, 28 October 2020

 
Author [[PageAuthor::Rim Halaby, M.D. [1] (Reviewed by Yazan Daaboul, M.D.)]]
Exam Type ExamType::USMLE Step 1
Main Category MainCategory::Biochemistry, MainCategory::Genetics
Sub Category SubCategory::Renal
Prompt [[Prompt::A 27-year-old man presents to the emergency department with severe left flank pain for the past 3 hours. He states the pain is a sharp, stabbing sensation that radiates to his left groin. Upon further questioning, the patient recalls that he has had similar episodes in the past. Physical examination is remarkable for left costovertebral angle tenderness. Urinalysis demonstrates hematuria and hexagonal-shaped crystals. Following further investigation, the physician explains to the patient that his condition is caused by a genetic disorder characterized by a mutation in an amino acid transporters in the kidneys. If genetic testing reveals the patient's wife does not carry a similar mutation, what is the percentage that this couple's child will have the disease?]]
Answer A AnswerA::0%
Answer A Explanation [[AnswerAExp::Cystinuria is an autosomal recessive disease. As the mother is not a carrier of the mutant allele (has 2 wild-type alleles), the couple's child would have had 0% chance of developing cystinuria and 100% chance of carrying a mutant allele.]]
Answer B AnswerB::25%
Answer B Explanation AnswerBExp::Had both the child's father and mother been carriers of the mutant allele, they would not have manifested the disease themselves, and their child would have had a 25% chance of developing cystinuria.
Answer C AnswerC::50%
Answer C Explanation [[AnswerCExp::Cystinuria is inherited in an autosomal recessive pattern. Patients who manifest the disease have 2 mutant alleles, while carriers of the mutation have only 1 mutant allele. The offspring of an individual with the disease and an individual who carries the allele has a 50% chance of developing the disease.]]
Answer D AnswerD::75%
Answer D Explanation AnswerDExp::Cystinuria is inherited in an autosomal recessive pattern. The couple's child has a 0% chance of developing cystinuria.
Answer E AnswerE::100%
Answer E Explanation AnswerEExp::An example of a 100% chance of a child developing cystinuria is when both parents have fully manifest disease (both carry 2 mutant alleles). In that case all offspring would have the disease too.
Right Answer RightAnswer::A
Explanation [[Explanation::The features of the patient's pain (location, radiation, and severity) and findings on physical examination (costovertebral angle tenderness), and urinalysis (hematuria and hexagonal-shaped crystals) are all consistent with the diagnosis of kidney stones (nephrolithiasis). In addition, the patient's recurrent presentation is concerning and warrants further investigation for an underlying etiology of his condition. Cystinuria is an autosomal recessive genetic disease characterized by reduced renal reabsorption of positively charged amino acids. It is caused by the presence of abnormal transporters in the kidneys for cysteine, ornithine, lysine, and arginine. Cystinuria results in impaired renal reabsorption and excessive excretion of these amino acids, and patients with cystinuria are predisposed to the development of recurrent cystine stones, which often manifest with hexagonal-shaped crystals on urinalysis. Given the autosomal recessive pattern of inheritance, the patient must have 2 copies of the mutant allele. Given that the mother is not a carrier of the mutant allele, There is a 100% chance that a child may be a silent carrier of the mutation, but a 0% chance that the disease will manifest phenotypically.

Educational Objective: Cystinuria is inherited in an autosomal recessive pattern. Patients who manifest the disease have 2 mutant alleles, while carriers of the mutation have only 1 mutant allele.
References: First Aid 2014 page 111]]

Approved Approved::Yes
Keyword WBRKeyword::Cystinuria, WBRKeyword::Cysteine, WBRKeyword::Cystine stone, WBRKeyword::Kidney stone, WBRKeyword::Nephrolithiasis, WBRKeyword::Autosomal recessive, WBRKeyword::Allele, WBRKeyword::Mutant, WBRKeyword::Hematuria, WBRKeyword::Flank pain
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