The condition may be diagnosed in utero or after the
The condition may be diagnosed in utero or after the
The skeleton produces blood cells. Red bone marrow contains stem cells that produce all of the blood cells.…
A 10-year-old boy is seen for evaluation of short stature and tibial deformity. His past medical history is notable for term birth with the following birth parameters: birth weight was 2460 grams (30 ng/ml), elevated alkaline phosphatase level (491 U/L; normal 100-325 U/L), normal calcium and phosphorous levels, and elevated spot urine N-terminal telopeptides (NTx; 574 nM BCE/mM Cr; normal 152-505 nM BCE/mM Cr). Bone mineral density by Dual-energy X-ray absorptiometry (DXA) showed a total body Z-score of -3.4 indicating bone mineral density below normal range. Molecular genetic testing identified a pathogenic mutation in the IFITM5 gene, confirming a diagnosis of osteogenesis imperfecta, type V.…
Your 80 year-old great aunt, Persis, was placing a canning jar on the top shelf of her pantry when she stepped awkwardly off the stool and twisted her leg at the hip. She felt a sharp pain in her hip and, after collapsing to the floor, found she could no longer stand. She was taken to the emergency room where an X ray showed that the neck of her femur was fractured. More detailed X ray images revealed reduced bone mass in the head and neck regions of the injured femur, in the ends of other long bones of the body and in the vertebrae. Surgery was necessary to repair the fractured femur and a biopsy of the bone tissue indicated that the composition of the osteoid was normal. Healing of the fractured femur is proceeding slowly.…
Shape and support of the human body is all due to our skeletal system. The curvature of the vertebrae column bones plays a major role in our upright posture. So people with bone conditions like osteogenesis imperfecta (genetic malformation) where the skeletal system are poorly formed, the patients are not just prone to fractures but have poorly moulded bones and irregular postures.…
Affecting only one in every 2 million people Fibrodysplasia ossificans progressiva (FOP) is one of the rarest genetic disorders of congenital skeleton malformations; identified by congenital malformation of the big toe at birth. Flare-ups occur by soft tissue injury followed by immobility. A mutation in the activin receptor IA/activin-like kinase 2 (ACVR1/ALK2), and bone protein (BMP) type I receptor were reported in all cases of FOP, making this a specific disease causing mutations in the human genome (Kaplan, 28 O). However, there is no current cure for FOP there are new developing treatments. The benefit to studying this rare disorder holds the key to discovering cures for other bone related disorders.…
A type of birth defect that affects the skeletal system is Spina Bifida. Spina Bifida is a nueral tube defect that occurs when the bones of the spine or the vertebrae do not form accurately around the spinal cord. In severe cases it can inhibit a persons walking or daily activities. There are three basic forms of Spina Bifida. The mildest form is Occulta, the next would be Meningocele and the most severe is Myelomeningocele. (http://www.uptodate.com/contents/overview-of-the-management-of-myelomeningocele-spina-bifida 2012) Myelomeningocele is the case that affects the skeletal system the most. With this, the nerves in the spine protrude out of the spinal canal and a bulge in the skin may appear. If nerves become damaged, there may be a high chance that there could be problems with walking, coordination and bowel…
Which is the main component of the connective tissue that gives the bones strength and support, but in this sickness is not found. This genetic disorder is extremely severed in the person that suffers from it and getting or fracturing them is very easily. They are 8 forms of this disorder, but the 2nd form being the deadliest, because it kills within the first year of life or at birth. For the baby might have severe bone deformity making hard to interior organs developed right. The other types have a lot in common but one is found in certain parts of other countries. Mostly pass down by a parent, but there are also cases that the defected is cause by a result of new genetic…
Sarah is Tommy’s cousin, and she has been experiencing muscle sorenss 24 to 72 hours after her initial workout. Tommy is a shot put athlete, who probably participates in advanced weight lifting workouts. Sarah thinks hyperplasia may be the cause of her severe muscle soreness. Hyperplasia is where the splitting of muscle fibers cell as a response to resistance training. Hyperplasia also allows for muscles to adapt to the resistance, and grow in size or increase in strength.…
Craniofrontonasal Dysplasia (CFND) is a rare, inherited x-linked disorder that results in deformities and abnormalities in the craniofacial area of those who are diagnosed with the disease. It is unusually more prevalent in females than in males and the symptoms tend to be more severe in females as well. Some of the many symptoms associated with this disease include widely spaced eyes, an unusually wide mouth, a cleft that is located on the tip of the nose, and other portions of the face may appear to be underdeveloped. Also, patients tend to have webbed feet and hands. While this disease can be detected in prenatal exams, the only treatment to resolve it appears to be mainly constructive in that surgery can be used to address some of the…
Fibromuscular dysplasia (FMD) is currently defined as an idiopathic, segmental, non-inflammatory and non-atherosclerotic disease of the musculature of arterial walls, leading to stenosis of small and medium-sized arteries.[1] The prevalence of FMD is not precisely known. Several studies determined prevalence in arteriograms of potential kidney donors. Craig et al reviewed the results of 1,862 renal angiograms obtained in potential renal donors and found FMD in 71 patient (3.8%).[2] In another study of 159 potential renal donors, 7 had FMD (4.4%).[3] Blondin et al found four cases of fibromuscular dysplasia (3.9%) in 101 renal donors.[4] In 2012 first 447 patients were enrolled in The United States Registry for Fibromuscular Dysplasia. [5] No studies have investigated the prevalence of…
Muscular dystrophy is a genetic disorder. It is inherited just like height and eye color. Scientists now know that a defective gene causes each type of muscular dystrophy. In…
A 6-year-old female born with Spondyloepiphyseal dysplasia (SED) was diagnosed with a complex deformity within her cervical spinal region. Her surgeon needed a biomodel detailing the cervical region of C0 to C1/2, which is the upper region of the spine and base of the skull. SED is an inheritable bone dysplasia causing abnormalities that are formed during birth. Characteristics of this bone dysplasia and SED include underdevelopment and fragmentation of the bone and cartilage of the epiphyses, which are the rounded ends or “heads” of the long bones, and underdevelopment of the vertebrae in the spine. Her physical symptoms included growth deficiency occurring before birth and continuing through childhood resulting in a disproportionate short…
Directions: This is not a typical research paper that can be copy/pasted/plagiarized. In this assignment, you will personalize your search for learning more about an…
This condition is usually inherited as autosomal dominant characteristic. There are two type of polydactyly; the pre-axial (extra digit towards the hand or foot) and post-axial (extra digit is towards the lateral margin of the hand or foot). Polydactyl can occur at the same time when excess digits are fused together, which is called polysndactyly. Patients with polydactyl can exhibit Werner mesomelic syndrome. This condition is characterised by a short limb dwarfism as a result of hypoplastic tibia. WMS occurs due to specific point mutation at position 404. (Cho et al., 2013) patients with WMS, can also exhibit duplication of the ZRS region, which is the cause of type Haas polysyndactyly or triphalangeal thumb polysyndactyly syndrome. This condition doesn’t affect lower limb development. This suggests that different mutational mechanisms affecting the enhancer region of the shh gene demonstrate different phenotypic outcomes. (Wieczorek et al.,…
One of the most terrifying and frightening words in the English language is cancer. Many children and adults of all ages can be diagnosed with a rare type of bone cancer each year. The harmful effects of this disease cannot only be detrimental but deadly too. Thus, with early detection, diagnosis, and proper treatment, individuals have a better chance of survival when treated early.…