Extracellular matrix components — MCQs

A 15-year-old boy presents with shortness of breath on exertion for the past 2 weeks. Although he does not have any other complaints, he is concerned about not gaining much weight despite a good appetite. His height is 188 cm (6 ft 2 in) and weight is 58 kg (124 lb). His blood pressure is 134/56 mm Hg and his pulse rate is 78/min. On cardiac auscultation, his apex beat is displaced laterally with a diastolic murmur lateral to the left sternal border. Slit-lamp examination shows an upward and outward displacement of both lenses. Synthesis of which of the following proteins is most likely defective in this patient?

Collagen is a very critical structural protein in many of our connective tissues. Defects in collagen produce diseases such as Ehlers-Danlos syndrome, where there is a defective lysyl hydroxylase gene, or osteogenesis imperfecta, where there is a defect in the production of type I collagen. Which of the following represents the basic repeating tripeptide of collagen?

A 62-year-old man with prostate cancer comes to the physician because of low back pain for 2 weeks and a 4.5-kg (10-lb) weight loss. Physical examination shows localized tenderness over the lumbar spine. An x-ray of the lumbar spine shows several osteoblastic lesions at the level of L2 and L4 vertebrae. Microscopic examination of a bone biopsy specimen from the L4 vertebra shows irregular bone trabeculae and star-shaped cells with long, cytoplasmic processes located deep within the lacunae. Exchange of nutrients and waste products between these cells most likely occurs through which of the following structures?

A 6-year-old boy with a history of multiple fractures is brought to his pediatrician by his mother, because she is concerned her child cannot hear her. On physical exam, kyphoscoliosis, poor dentition, bowing of long bones, and conductive hearing loss is noted. On genetic analysis, the patient has a COL1A1 gene mutation. The defect found in this patient is most likely associated with impaired formation of which of the following?

A 4-year-old boy is brought to the physician for a well-child examination. He started walking at 20 months of age. He can use a cup to drink but cannot use silverware. He speaks in 2-word sentences and can build a tower of 4 blocks. He can scribble but cannot draw a circle. He is above the 99th percentile for height and at the 15th percentile for weight. Vital signs are within normal limits. Examination shows bilateral inferior lens dislocation. His fingers are long and slender. He has a high-arched palate. The thumb and 5th finger overlap when he grips a wrist with the opposite hand. The skin over the neck can be extended and stretched easily. Which of the following is the most likely cause of these findings?

A 5-year-old boy presents to a pediatric orthopedic surgeon for evaluation of spinal curvature. His primary care physician noticed during an annual checkup that the boy's shoulders were uneven, and radiograph revealed early onset scoliosis. His past medical history is significant for multiple fractures as well as short stature. Based on the early presentation of scoliosis and the unusual history of fractures, the surgeon orders further workup and discovers a genetic mutation in an extracellular protein. This protein exists in two different forms. The first is an insoluble dimer that is linked by disulfide bonds and links integrins to the extracellular matrix. The second is a soluble protein that assists with clotting. Based on these descriptions, which of the following proteins is most likely mutated in this patient?

A 69-year-old man comes to the physician with a 2-year history of progressive hearing loss. His hearing is worse in crowded rooms, and he has noticed that he has more difficulty understanding women than men. He has no history of serious illness and does not take any medications. A Rinne test shows air conduction is greater than bone conduction bilaterally. This condition is most likely associated with damage closest to which of the following structures?

A 3-month-old infant presents with severe joint hypermobility, skin hyperextensibility, and delayed wound healing. Skin biopsy shows abnormal collagen fibril organization with irregular diameter and reduced tensile strength. Genetic testing reveals a mutation affecting lysyl hydroxylase, an enzyme involved in collagen post-translational modification. The family asks about prognosis and potential complications. Synthesize the biochemical defect with clinical manifestations to determine the most critical pathophysiological mechanism.

A 58-year-old woman undergoes cervical biopsy following an abnormal Pap smear. Histology shows full-thickness epithelial atypia with loss of cellular polarity, increased nuclear-to-cytoplasmic ratio, and numerous mitotic figures, but the basement membrane remains intact. Her oncologist discusses treatment options. The patient is concerned about progression risk versus overtreatment. Evaluate the most appropriate management strategy considering the tissue diagnosis and natural history.

A 42-year-old woman with Marfan syndrome presents to the emergency department with acute chest pain. CT angiography reveals a Type A aortic dissection. The cardiothoracic surgeon explains that her underlying connective tissue disorder predisposed her to this complication. During surgery, the aortic wall appears thin and fragile. Evaluate which molecular defect best explains the compromised structural integrity of her aortic wall.