Genetic and Metabolic Disorders Practice Questions

Q: All of the following are true about Down syndrome except for one.

Incidence of Robertsonian translocation is 1:1000. **Incidence of Robertsonian translocation is 1:1000** - This statement is **not accurate** for Down syndrome. Robertsonian translocation accounts for only about **3-4% of Down syndrome cases**, not a general population incidence of 1:1000. - The vast majority of Down syndrome cases (~95%) are due to trisomy 21 from nondisjunction, not translocation. - This is the **correct answer** as it is the FALSE statement. *Extra chromosome is of maternal origin* - In approximately **90-95% of Down syndrome cases**, the extra copy of chromosome 21 originates from the mother due to **nondisjunction** during meiosis. - This maternal origin is strongly correlated with **advanced maternal age**. *Most common cause is trisomy 21* - **Trisomy 21** (due to meiotic nondisjunction) accounts for about **95% of all Down syndrome cases**, making it the most common genetic mechanism. - This results in three separate copies of chromosome 21 in all body cells. *Mosaicism 21 has no association with maternal age* - **Mosaic Down syndrome** occurs when nondisjunction happens *after fertilization* in early embryonic development, leading to a mixture of cells with normal and trisomic cells. - Because it is a **post-zygotic event**, its incidence is independent of **maternal age**, unlike full trisomy 21. *Incidence increases with advanced maternal age* - **TRUE statement** - The risk of Down syndrome (particularly trisomy 21) increases significantly with **maternal age**. - Risk is approximately 1:1500 at age 20, 1:1000 at age 30, 1:400 at age 35, and 1:100 at age 40. - This is due to increased risk of meiotic nondisjunction in older oocytes.

Q: Which of the following is not a typical symptom of Duchenne Muscular Dystrophy (DMD)?

Tenderness in muscles. ***Tenderness in muscles*** - **Muscle tenderness** and pain are **not typical primary symptoms** of Duchenne Muscular Dystrophy (DMD); the disease is characterized by progressive muscle weakness without significant pain. - While some discomfort might arise from muscle spasms or joint issues, widespread tenderness is characteristic of inflammatory conditions, not DMD. *Muscle pseudo hypertrophy* - **Pseudohypertrophy**, particularly in the calves, is a **hallmark sign** of DMD, caused by the replacement of muscle tissue with fat and connective tissue, making the muscles appear larger but weaker. - This symptom reflects the underlying muscle degeneration in DMD. *Muscle weakness* - **Progressive muscle weakness** is the defining characteristic of DMD, typically starting in the proximal muscles and leading to significant functional impairment. - This weakness is due to the lack of **dystrophin**, which is crucial for muscle fiber integrity. *Cardiomyopathy* - **Cardiomyopathy** is a **common and serious complication** of DMD, affecting nearly all patients by adolescence or early adulthood due to the absence of dystrophin in cardiac muscle. - It often manifests as **dilated cardiomyopathy**, contributing significantly to morbidity and mortality. *Gower's sign* - **Gower's sign** is a **classic clinical manifestation** of DMD, where the child uses their hands to "walk up" their legs when rising from the floor due to proximal muscle weakness. - This sign typically appears early in the disease course and is a key diagnostic indicator.

Q: In which condition is the presence of an extra pair of ribs sometimes observed?

Turner syndrome. ***Turner syndrome*** - **Turner syndrome** (45,X) is often associated with skeletal abnormalities, including an extra pair of ribs (cervical ribs) in some cases. - Other common skeletal features include **short stature**, a **shield chest**, and **cubitus valgus**. *Down syndrome* - **Down syndrome** (trisomy 21) is characterized by specific facial features, intellectual disability, and congenital heart defects. - While it can manifest with various skeletal anomalies, an extra pair of ribs is not a characteristic feature. *Klinefelter syndrome* - **Klinefelter syndrome** (47,XXY) is characterized by hypogonadism, tall stature, gynecomastia, and learning difficulties. - Skeletal features may include long limbs and decreased bone density, but cervical ribs are not typically associated with this condition. *Holt-Oram syndrome* - **Holt-Oram syndrome** is a genetic disorder affecting heart and limb development, specifically the upper limbs (thumb abnormalities, phocomelia). - It does not typically involve the presence of an extra pair of ribs. *Fibrous dysplasia* - **Fibrous dysplasia** is a bone disorder where normal bone is replaced by fibrous tissue, leading to weakened bone and fractures. - It is a localized bone condition and does not involve the presence of supernumerary ribs.

Q: Which of the following is not typically associated with Treacher Collins syndrome?

Choanal atresia. Choanal atresia - While Treacher Collins syndrome involves various craniofacial anomalies, **choanal atresia** (blockage of the nasal airway) is **not a typical** or defining feature. - Choanal atresia is more commonly associated with conditions like **CHARGE syndrome** or isolated congenital defects. *Conductive deafness* - **Conductive deafness** is a common feature of Treacher Collins syndrome due to malformations of the **ossicles** and external ear structures. - The abnormal development of middle ear components prevents proper sound transmission, occurring in approximately **50% of cases**. *Cleft palate* - Although less frequent than other features, a **cleft palate** can occur in some individuals with Treacher Collins syndrome, especially in more severe cases. - It results from incomplete fusion of the palatal shelves during embryonic development, occurring in approximately **28-35% of cases**. *Mandibular hypoplasia* - **Mandibular hypoplasia** (underdevelopment of the jaw) is a **hallmark characteristic** of Treacher Collins syndrome, leading to a small chin and retrognathia. - This often contributes to feeding and breathing difficulties in affected individuals. *Malar hypoplasia* - **Malar hypoplasia** (underdevelopment of the cheekbones) is a **classic and defining feature** of Treacher Collins syndrome. - This results in flattened cheeks and contributes to the characteristic facial appearance of the condition.

Q: What is the name of the syndrome associated with the deletion of chromosome 22?

Di George syndrome. ***Di George syndrome*** - Di George syndrome, also known as **22q11.2 deletion syndrome**, is caused by a deletion on the long arm of chromosome 22. - This syndrome is associated with varied clinical features, including **congenital heart defects**, **thymic hypoplasia** (leading to immune deficiencies), **hypocalcemia** due to parathyroid hypoplasia, and characteristic facial features. *Down syndrome* - Down syndrome is caused by a **trisomy of chromosome 21**, meaning there's an extra copy of chromosome 21. - It is characterized by intellectual disability, distinctive facial features, and developmental delays, and is not associated with chromosome 22 deletion. *Turner syndrome* - Turner syndrome is a chromosomal condition affecting females, characterized by the partial or complete absence of one of the **X chromosomes (45, X0)**. - It leads to short stature, ovarian dysfunction, and characteristic physical features, unrelated to chromosome 22. *Klinefelter syndrome* - Klinefelter syndrome is a chromosomal disorder in males resulting from an extra **X chromosome (47, XXY)**. - Individuals often experience hypogonadism, reduced fertility, and abnormal body proportions, which is distinct from a deletion on chromosome 22. *Prader-Willi syndrome* - Prader-Willi syndrome is caused by a **deletion of paternal chromosome 15q11-q13** or maternal uniparental disomy. - It presents with hypotonia, hyperphagia, obesity, intellectual disability, and hypogonadism, unrelated to chromosome 22 deletion.

Q: Which of the following is not a characteristic of Fragile X syndrome?

Large nose. **Large nose** - **Large nose** is generally not considered a characteristic feature of **Fragile X syndrome**. - While individuals with Fragile X syndrome have distinct facial features, a prominent or large nose is not typically among them. *Large head* - **Macrocephaly** (large head circumference) is a recognized physical feature in many individuals with **Fragile X syndrome**. - This characteristic often becomes more apparent in infancy and childhood. *Large ear* - **Large, prominent ears** are a very common and classic physical characteristic observed in individuals with **Fragile X syndrome**. - This feature is often noted during developmental assessments. *Large testis* - **Macro-orchidism** (enlarged testes) is a hallmark physical characteristic of **Fragile X syndrome** in post-pubertal males. - This is a highly specific finding and a key diagnostic pointer for the syndrome in adolescent and adult males. *Long narrow face* - **Long, narrow face** with a prominent forehead and jaw is a typical facial feature of **Fragile X syndrome**. - This characteristic facial appearance is part of the recognizable phenotype of the syndrome.

Q: Which of the following is NOT a characteristic of LEOPARD syndrome?

Hypergonadism. ***Hypergonadism*** - **LEOPARD syndrome** is characterized by **hypogonadism** (underdevelopment or dysfunction of the gonads) and delayed puberty, not hypergonadism. - The acronym LEOPARD stands for multiple clinical features which include **L**entigines, **E**CG conduction abnormalities, **O**cular hypertelorism, **P**ulmonary stenosis, **A**bnormal genitalia, **R**etardation of growth, and **D**eafness. *Growth retardation* - **Retardation of growth** is a defining characteristic of LEOPARD syndrome, often manifesting as short stature. - This is part of the "R" in the LEOPARD acronym, indicating a failure to achieve normal growth milestones. *ECG changes* - **ECG conduction abnormalities** (such as prolonged PR interval, bundle branch block, or Wolff-Parkinson-White syndrome) are primary diagnostic features. - These cardiac issues can be significant and contribute to the morbidity associated with the syndrome. *Hypertelorism* - **Ocular hypertelorism**, meaning widely spaced eyes, is a common facial dysmorphism found in individuals with LEOPARD syndrome. - This feature is represented by the "O" in the LEOPARD acronym, along with other craniofacial anomalies. *Lentigines* - **Lentigines** are multiple pigmented macules (small, flat, darkened spots) that are the hallmark dermatologic feature of LEOPARD syndrome. - These represent the "L" in the LEOPARD acronym and are typically present from early childhood, increasing in number with age.

Q: Which is the most common genetic cause of mental retardation?

Fragile X syndrome. ***Fragile X syndrome*** - This is the most common **inherited cause** of **intellectual disability** and the second most common overall genetic cause after **Down syndrome**. - It is caused by an expansion of the **CGG trinucleotide repeat** in the **FMR1 gene** on the X chromosome, leading to reduced or absent **Fragile X Mental Retardation Protein (FMRP)**. - In the context of **inherited** genetic causes (following Mendelian inheritance patterns), Fragile X is the most prevalent. *Down syndrome* - This is the most common **overall genetic cause** of intellectual disability, occurring in approximately **1 in 700 live births**. - It is caused by **trisomy 21** (an extra copy of chromosome 21), typically due to nondisjunction during meiosis. - While it is a genetic cause, it is usually a **de novo chromosomal abnormality** rather than an inherited condition, which distinguishes it from Fragile X syndrome. *Tuberous sclerosis* - This is a neurocutaneous disorder characterized by **non-malignant tumors** in multiple organs, including the brain, skin, and kidneys. - While it can cause intellectual disability, it is not the most common genetic cause; its prevalence is lower than Fragile X syndrome. *Cri-du-chat syndrome* - This syndrome is caused by a **deletion** on the **short arm of chromosome 5** and is characterized by a distinctive **cat-like cry** in infancy, intellectual disability, and microcephaly. - While it causes intellectual disability, it is rarer than Fragile X syndrome. *Angelman syndrome* - This syndrome is a neurodevelopmental disorder typically caused by a **deletion or mutation** on the maternal copy of **chromosome 15q11-q13**, or **paternal uniparental disomy**. - It presents with severe developmental delay, **ataxia**, **seizures**, and a happy demeanor, but it is less common than Fragile X syndrome as a genetic cause of mental retardation.

Q: Cystic hygroma is associated with which of the following syndromes?

Turner syndrome. ***Turner syndrome*** - **Cystic hygroma** is a common Fetal anomaly associated with **Turner syndrome (45,X)**, which is characterized by a single X chromosome. - The cystic hygroma in Turner syndrome is thought to arise from abnormal development of the **lymphatic system**, leading to large lymphatic cysts, particularly in the neck. *Klinefelter syndrome* - **Klinefelter syndrome (47,XXY)** is characterized by an extra X chromosome in males and is typically associated with **testicular atrophy**, **gynecomastia**, and tall stature. - It is **not commonly associated** with cystic hygroma. *Marfan syndrome* - **Marfan syndrome** is an autosomal dominant disorder affecting **connective tissue**, primarily impacting the skeletal, ocular, and cardiovascular systems. - It is characterized by **tall stature**, **arachnodactyly**, **lens dislocation**, and **aortic root dilation**, but not cystic hygroma. *Down syndrome* - **Down syndrome (Trisomy 21)** is characterized by an extra copy of chromosome 21 and is associated with distinct facial features, **intellectual disability**, and various congenital anomalies. - While other anomalies like **duodenal atresia** and **congenital heart defects** (e.g., AVSD) are common, **cystic hygroma is not a primary association** of Down syndrome; it is more characteristic of Turner syndrome. *Patau syndrome* - **Patau syndrome (Trisomy 13)** is characterized by an extra copy of chromosome 13 and is associated with severe intellectual disability, **cleft lip/palate**, **polydactyly**, **holoprosencephaly**, and congenital heart defects. - Cystic hygroma is **not a typical feature** of Patau syndrome.

Question 1

All of the following are true about Down syndrome except for one.

Accepted Answer

Incidence of Robertsonian translocation is 1:1000

Answer

Most common cause is trisomy 21

Answer

Mosaicism 21 has no association with maternal age

Answer

Extra chromosome is of maternal origin

Answer

Incidence increases with advanced maternal age

Question 2

Which of the following is not a typical symptom of Duchenne Muscular Dystrophy (DMD)?

Accepted Answer

Tenderness in muscles

Answer

Muscle pseudo hypertrophy

Answer

Muscle weakness

Answer

Cardiomyopathy

Answer

Gower's sign

Question 3

In which condition is the presence of an extra pair of ribs sometimes observed?

Accepted Answer

Turner syndrome

Answer

Down syndrome

Answer

Holt-Oram syndrome

Answer

Fibrous dysplasia

Answer

Klinefelter syndrome

Question 4

Which of the following is not typically associated with Treacher Collins syndrome?

Accepted Answer

Choanal atresia

Answer

Conductive deafness

Answer

Cleft palate

Answer

Mandibular hypoplasia

Answer

Malar hypoplasia

Question 5

What is the name of the syndrome associated with the deletion of chromosome 22?

Accepted Answer

Di George syndrome

Answer

Down syndrome

Answer

Turner syndrome

Answer

Klinefelter syndrome

Answer

Prader-Willi syndrome

Question 6

Which of the following is not a characteristic of Fragile X syndrome?

Accepted Answer

Large nose

Answer

Large ear

Answer

Large testis

Answer

Large head

Answer

Long narrow face

Question 7

Which of the following is NOT a characteristic of LEOPARD syndrome?

Accepted Answer

Hypergonadism

Answer

Growth retardation

Answer

ECG changes

Answer

Hypertelorism

Answer

Lentigines

Question 8

Which is the most common genetic cause of mental retardation?

Accepted Answer

Fragile X syndrome

Answer

Tuberous sclerosis

Answer

Cri-du-chat syndrome

Answer

Angelman syndrome

Answer

Down syndrome

Question 9

A child with microcephaly, blue eyes, fair skin, and intellectual disability is likely to have:

Accepted Answer

Phenylketonuria (PKU)

Answer

Homocystinuria

Answer

Tyrosinosis

Answer

Alkaptonuria

Answer

Maple syrup urine disease

Question 10

Cystic hygroma is associated with which of the following syndromes?

Accepted Answer

Turner syndrome

Answer

Klinefelter syndrome

Answer

Marfan syndrome

Answer

Down syndrome

Answer

Patau syndrome

Genetic and Metabolic Disorders — MCQs

Genetic and Metabolic Disorders — MCQs

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