Which are the symptoms of Smith-Lemli-Opitz Syndrome?

Smith-Lemli-Opitz Syndrome: Symptoms and Characteristics

Smith-Lemli-Opitz Syndrome (SLOS) is a rare genetic disorder that affects multiple systems in the body. It is caused by mutations in the DHCR7 gene, which is responsible for producing an enzyme called 7-dehydrocholesterol reductase. This enzyme plays a crucial role in the synthesis of cholesterol, a vital component of cell membranes and a precursor for various hormones and molecules in the body.

Individuals with Smith-Lemli-Opitz Syndrome have impaired cholesterol metabolism, leading to a wide range of physical, developmental, and cognitive symptoms. The severity of the condition can vary significantly from person to person, even among affected individuals within the same family.

Physical Features:

One of the most distinctive physical features of Smith-Lemli-Opitz Syndrome is facial dysmorphism, which refers to abnormal facial characteristics. These may include a small head (microcephaly), a prominent forehead, widely spaced eyes (hypertelorism), a small nose with a broad nasal bridge, a thin upper lip, and a small chin. Additionally, individuals with SLOS may have malformed ears, including low-set ears or ears with unusual shape or folding.

Growth and Development:

Children with Smith-Lemli-Opitz Syndrome often experience growth delays, both prenatally and postnatally. They may have a low birth weight and height, and their growth may continue to be slower than average throughout childhood. Delayed development is also common, with affected individuals often experiencing delays in reaching developmental milestones such as sitting, crawling, walking, and talking.

Intellectual and Cognitive Impairments:

Smith-Lemli-Opitz Syndrome can cause a wide range of intellectual and cognitive impairments. Most individuals with SLOS have some degree of intellectual disability, ranging from mild to severe. They may have learning difficulties, impaired problem-solving skills, and challenges with attention and concentration. Additionally, individuals with SLOS may exhibit behavioral issues such as hyperactivity, impulsivity, and self-injurious behaviors.

Organ and Systemic Abnormalities:

SLOS can affect various organs and systems in the body, leading to additional symptoms and complications. Some common abnormalities include:

• Cardiac Abnormalities: Approximately 50% of individuals with SLOS have congenital heart defects, such as ventricular septal defects (holes in the heart) or abnormalities in the structure of the heart.


• Genital Abnormalities: Both males and females with Smith-Lemli-Opitz Syndrome may have genital abnormalities. Males may have undescended testicles (cryptorchidism) or hypospadias (a condition where the opening of the urethra is on the underside of the penis). Females may have an enlarged clitoris or other malformations of the reproductive organs.


• Gastrointestinal Issues: Some individuals with SLOS may experience feeding difficulties, gastroesophageal reflux disease (GERD), or constipation.


• Respiratory Problems: Respiratory issues, such as recurrent respiratory infections, breathing difficulties, and asthma, can occur in individuals with Smith-Lemli-Opitz Syndrome.


• Skeletal Abnormalities: Skeletal abnormalities, including extra fingers or toes (polydactyly), fused fingers or toes (syndactyly), or joint contractures, may be present in some individuals with SLOS.

Other Possible Symptoms:

While the aforementioned symptoms are commonly associated with Smith-Lemli-Opitz Syndrome, it is important to note that not all individuals will exhibit every symptom. Some additional features that may be present in individuals with SLOS include cleft palate, kidney abnormalities, hearing loss, vision problems, seizures, and abnormal tooth development.

Conclusion:

Smith-Lemli-Opitz Syndrome is a complex genetic disorder that affects multiple aspects of an individual's health and development. The symptoms can vary widely in severity and presentation, making each case unique. Early diagnosis and intervention are crucial in managing the condition and providing appropriate support and care for affected individuals and their families.

by Diseasemaps