WBR0318: Difference between revisions
Jump to navigation
Jump to search
No edit summary |
No edit summary |
||
| Line 8: | Line 8: | ||
|MainCategory=Pathology | |MainCategory=Pathology | ||
|SubCategory=Neurology | |SubCategory=Neurology | ||
|MainCategory=Pathology | |||
|MainCategory=Pathology | |MainCategory=Pathology | ||
|MainCategory=Pathology | |MainCategory=Pathology | ||
| Line 22: | Line 23: | ||
|Prompt=A 6-month-old male is brought by his mother to the physician's office for failure to thrive. Following appropriate work-up, that patient is diagnosed with a disease that is characterized by an inability to phosphorylate mannose residues on glycoproteins, leading to the aggregation of a variety of substrates in the extracellular matrix. Which of the following clinical features are most likely to be present in this patient? | |Prompt=A 6-month-old male is brought by his mother to the physician's office for failure to thrive. Following appropriate work-up, that patient is diagnosed with a disease that is characterized by an inability to phosphorylate mannose residues on glycoproteins, leading to the aggregation of a variety of substrates in the extracellular matrix. Which of the following clinical features are most likely to be present in this patient? | ||
|Explanation=The patient is most likely presenting with inclusion cell disease, also known as I-cell disease (mucolipidosis type II), a lysosomal storage disease characterized by a defective phosphorylation of mannose residues. This occurs due to a defect of GlcNAc-phosphotransferase, which is normally found on the Golgi apparatus. Consequently, lysosomal enzymes are secreted out of the cell, rather than being directed to the lysosomes. Typical manifestations of I-cell disease are coarse facial features, restricted joint movement, and clouded corneas in very young children, which all result from the aggregation of substances that normally would be degraded in the lysosomes. I-cell disease is usually deadly in childhood. | |Explanation=The patient is most likely presenting with inclusion cell disease, also known as I-cell disease (mucolipidosis type II), a lysosomal storage disease characterized by a defective phosphorylation of mannose residues. This occurs due to a defect of GlcNAc-phosphotransferase, which is normally found on the Golgi apparatus. Consequently, lysosomal enzymes are secreted out of the cell, rather than being directed to the lysosomes. Typical manifestations of I-cell disease are coarse facial features, restricted joint movement, and clouded corneas in very young children, which all result from the aggregation of substances that normally would be degraded in the lysosomes. I-cell disease is usually deadly in childhood. | ||
|AnswerA=Clouded corneas and restricted joint movement | |AnswerA=Clouded corneas and restricted joint movement | ||
|AnswerAExp= See explination. | |AnswerAExp=See explination. | ||
|AnswerB=Partial albinism and peripheral neuropathy | |AnswerB=Partial albinism and peripheral neuropathy | ||
|AnswerBExp=[[Chediak-Higashi syndrome]] is a disease characterized by the 3Ps: Peripheral neuropathy, Peripheral neuropathy, and Pyogenic infections. [[Chediak-Higashi syndrome]] occurs as a result of a lysosomal trafficking regular gene mutation. | |AnswerBExp=[[Chediak-Higashi syndrome]] is a disease characterized by the 3Ps: Peripheral neuropathy, Peripheral neuropathy, and Pyogenic infections. [[Chediak-Higashi syndrome]] occurs as a result of a lysosomal trafficking regular gene mutation. | ||
|AnswerC=Situs inversus and bronchiectasis | |AnswerC=Situs inversus and bronchiectasis | ||
|AnswerCExp= [[Kartagener's syndrome]] or primary ciliary dyskinesia is often characterized by infertility, bronchiectasis, sinusitis, and is often associated with situs inversus. [[Kartagener's syndrome]] occurs as a result of a dynein arm defect. | |AnswerCExp=[[Kartagener's syndrome]] or primary ciliary dyskinesia is often characterized by infertility, bronchiectasis, sinusitis, and is often associated with situs inversus. [[Kartagener's syndrome]] occurs as a result of a dynein arm defect. | ||
|AnswerD=Thymic aplasia and recurrent infections | |AnswerD=Thymic aplasia and recurrent infections | ||
|AnswerDExp= Severe combined immunodeficiency is often characterized by [[thymic aplasia]] and recurrent infections (bacterial, viral, fungal, and protozoal). It occurs as a result of a defective interleukin-2 receptor or adenosine deaminase deficiency. | |AnswerDExp=Severe combined immunodeficiency is often characterized by [[thymic aplasia]] and recurrent infections (bacterial, viral, fungal, and protozoal). It occurs as a result of a defective interleukin-2 receptor or adenosine deaminase deficiency. | ||
|AnswerE=Hepatomegaly and aseptic necrosis of the femur | |AnswerE=Hepatomegaly and aseptic necrosis of the femur | ||
|AnswerEExp= [[Gaucher's disease]], a lysosomal storage disease, is often characterized by hepatomegaly and aseptic necrosis of the femur. On pathology, Gaucher's cells ("crumpled tissue paper" macrophages) are observed. | |AnswerEExp=[[Gaucher's disease]], a lysosomal storage disease, is often characterized by hepatomegaly and aseptic necrosis of the femur. On pathology, Gaucher's cells ("crumpled tissue paper" macrophages) are observed. | ||
|EducationalObjectives=Clinical features of I-cell disease are coarse facial features, clouded corneas, and restricted joint movement, which all result from the aggregation of substances that normally would be degraded in the lysosomes. | |||
|References=First Aid 2014 page 77 | |||
|RightAnswer=A | |RightAnswer=A | ||
|WBRKeyword=restricted, joint, movement, I-cell, i, cell, disease, inclusion, cell, disease, inclusion, mannose-6-phophase, mannose, phosphate, 6, lysosome, lysosomes, lysosomal, protein, proteins, mucolipidosis, coarse, facial, feature, features | |WBRKeyword=restricted, joint, movement, I-cell, i, cell, disease, inclusion, cell, disease, inclusion, mannose-6-phophase, mannose, phosphate, 6, lysosome, lysosomes, lysosomal, protein, proteins, mucolipidosis, coarse, facial, feature, features | ||
|Approved=Yes | |Approved=Yes | ||
}} | }} | ||
Revision as of 16:53, 14 September 2014
| Author | [[PageAuthor::Rim Halaby, M.D. [1] (Reviewed by Alison Leibowitz)]] |
|---|---|
| Exam Type | ExamType::USMLE Step 1 |
| Main Category | MainCategory::Pathology |
| Sub Category | SubCategory::Neurology |
| Prompt | [[Prompt::A 6-month-old male is brought by his mother to the physician's office for failure to thrive. Following appropriate work-up, that patient is diagnosed with a disease that is characterized by an inability to phosphorylate mannose residues on glycoproteins, leading to the aggregation of a variety of substrates in the extracellular matrix. Which of the following clinical features are most likely to be present in this patient?]] |
| Answer A | AnswerA::Clouded corneas and restricted joint movement |
| Answer A Explanation | AnswerAExp::See explination. |
| Answer B | AnswerB::Partial albinism and peripheral neuropathy |
| Answer B Explanation | [[AnswerBExp::Chediak-Higashi syndrome is a disease characterized by the 3Ps: Peripheral neuropathy, Peripheral neuropathy, and Pyogenic infections. Chediak-Higashi syndrome occurs as a result of a lysosomal trafficking regular gene mutation.]] |
| Answer C | AnswerC::Situs inversus and bronchiectasis |
| Answer C Explanation | [[AnswerCExp::Kartagener's syndrome or primary ciliary dyskinesia is often characterized by infertility, bronchiectasis, sinusitis, and is often associated with situs inversus. Kartagener's syndrome occurs as a result of a dynein arm defect.]] |
| Answer D | AnswerD::Thymic aplasia and recurrent infections |
| Answer D Explanation | [[AnswerDExp::Severe combined immunodeficiency is often characterized by thymic aplasia and recurrent infections (bacterial, viral, fungal, and protozoal). It occurs as a result of a defective interleukin-2 receptor or adenosine deaminase deficiency.]] |
| Answer E | AnswerE::Hepatomegaly and aseptic necrosis of the femur |
| Answer E Explanation | [[AnswerEExp::Gaucher's disease, a lysosomal storage disease, is often characterized by hepatomegaly and aseptic necrosis of the femur. On pathology, Gaucher's cells ("crumpled tissue paper" macrophages) are observed.]] |
| Right Answer | RightAnswer::A |
| Explanation | [[Explanation::The patient is most likely presenting with inclusion cell disease, also known as I-cell disease (mucolipidosis type II), a lysosomal storage disease characterized by a defective phosphorylation of mannose residues. This occurs due to a defect of GlcNAc-phosphotransferase, which is normally found on the Golgi apparatus. Consequently, lysosomal enzymes are secreted out of the cell, rather than being directed to the lysosomes. Typical manifestations of I-cell disease are coarse facial features, restricted joint movement, and clouded corneas in very young children, which all result from the aggregation of substances that normally would be degraded in the lysosomes. I-cell disease is usually deadly in childhood. Educational Objective: Clinical features of I-cell disease are coarse facial features, clouded corneas, and restricted joint movement, which all result from the aggregation of substances that normally would be degraded in the lysosomes. |
| Approved | Approved::Yes |
| Keyword | WBRKeyword::restricted, WBRKeyword::joint, WBRKeyword::movement, WBRKeyword::I-cell, WBRKeyword::i, WBRKeyword::cell, WBRKeyword::disease, WBRKeyword::inclusion, WBRKeyword::cell, WBRKeyword::disease, WBRKeyword::inclusion, WBRKeyword::mannose-6-phophase, WBRKeyword::mannose, WBRKeyword::phosphate, WBRKeyword::6, WBRKeyword::lysosome, WBRKeyword::lysosomes, WBRKeyword::lysosomal, WBRKeyword::protein, WBRKeyword::proteins, WBRKeyword::mucolipidosis, WBRKeyword::coarse, WBRKeyword::facial, WBRKeyword::feature, WBRKeyword::features |
| Linked Question | Linked:: |
| Order in Linked Questions | LinkedOrder:: |