A physical examination reveals the following: leonine facies; loss of eyebrows and eyelashes; nodules on the sclera; a depressed nasal bridge; adipose fat deposits in the breast; testicular atrophy; many symmetrical, flat, discolored areas on the skin without defined borders; numerous nodules & broad, raised areas on the skin; partial loss of pinprick and temperature sensation; no anhidrotic changes; symmetrically enlarged ulnar and common peroneal nerves.…
One main idea within the article is even though that Rosnick has Proteus syndrome, he does not let that stop him from achieving his goals. The fifth paragraph shows the amount of determination Rosnick had to achieve his goals by saying, “And Rosnick, large fingers and all, wanted to play baseball. So his father went to work dismantling and rebuilding baseball gloves, until one thing became clear. Just like Rosnick, now a senior at Champe High in Aldie, Virginia, had taught himself to tie his shoes and button his shirt, he was going to teach himself to be a true ballplayer - a pitcher at that.” First, Rosnick learned to tie his own shoe, and then, he learned to button on his own shirt, and lastly he set a goal of becoming a good pitcher which…
• a health condition that limits the blood supply(diabetes and peripheral arterial disease) making the skin vulnerable to bruising and damage…
A problem in the blood because an irregular hemoglobin. The cause of it is an inheritance.…
Paediatrics is the medical science related to the diagnosis and treatment of childhood illness. One of the illness such as Pierre Robin Syndrome (PRS) also called Pierre Robin Complex or Sequence was identified by Pierre Robin a French stomatologist in 1923. That is a facial difference condition with a very small lower jaw (micrognathia or retrognathia) (Figure 1), a normal size of tongue but in the setting of a very small jaw that the tongue looks large tends to fall a downward or backward-positioned toward the throat (glossoptosis)(Figure 2) can act as an obstruction and result in a U-shaped cleft palate presented at birth (birth defect) (Redett, 2008). This malformation development occurs in the womb and approximately one in 8,500 to 14,000…
Mr. Raphael is admitted for a twisting of the intestines. What is the medical term for this condition? Volvulus…
The patient is a 36 year old male who came to the hospital because of an episode of hematemesis. The patient stated that for the past few days he had had anorexia and epigastric pain, which was worse if he tried to eat. An NG tube was placed and drained a small amount of bright red blood, as well as some coffee-ground material. Hemoccult test showed dark, tarry stool and positive for occult blood.…
Aarskog syndrome (also known as Aarskog–Scott syndrome, faciodigitogenital syndrome, shawl scrotum syndrome and faciogenital dysplasia) is a rare autosomal X-linked inherited disorder that affects a person's height, muscles, skeleton, genitals, and appearance of the face. It mostly affects at birth and the symptoms usually become apparent by the age of 3years. Unfortunately, Aarskog syndrome is a lifelong condition without a cure. Some people with Aarskog syndrome are born with more serious abnormalities, such as heart defects or a cleft lip with or without an opening in the roof of the mouth (cleft palate). Most males with Aarskog syndrome have a shawl scrotum, in which the scrotum surrounds the penis. Less often, they have undescended testes (cryptorchidism) or a soft out-pouching around the belly-button (umbilical hernia) or in the lower abdomen (inguinal hernia).…
The patient is a 36 year old male who came to the hospital because of an episode of hematemesis. The patient stated that for the past few days he had had anorexia and epigastric pain, which was worse if he tried to eat. An NG tube was placed and drained a small amount of bright red blood, as well as some coffee-ground material. Hemoccult test showed dark, tarry stool and positive for occult blood. The patient is a 21 year old male who presented with a history of sudden onset of abdominal pain, first generalized, and then localizing to the RLQ. The pain was accompanied with anorexia and nausea. It has become increasingly more severe over the past 3 hours so that the patient now cannot walk. He had one episode of vomiting, and has a low-grade fever of 100. On examination the patient was in acute distress due to pain. Palpation of the abdomen showed generalized tenderness with marked pain in the RLQ and rebound pain. STAT CBC showed leukocytosis of 21,000. Abdominal ultrasound was ordered.…
Signs and Symptoms: Non-bullous impetigo is characterized by red sores that rupture and end up forming a golden crust on the affected area of the skin. 3 Symptoms can include mild itching and soreness and in more severe cases symptoms may include fever and swollen lymph nodes. 2…
OBJECTIVE: Patient appears as a well-developed female in no specific distress. Blood pressure 134/86, pulse 85, weight 168 pounds. Focused examination of the right arm reveals a small, circular lesion on the anterior forearm, most consistent with a seborrheic keratosis. This is pigmented and is popular.…
Caused by a build-up of fatty deposits on the walls of the arteries around the heart e.g pizza, sweets, chocolate…
There are several factors that contribute to the cause of BCC. These factors include, light colored skin, light colored eyes, blonde or red hair, overexposure to x-rays or radiation, many moles, genetics, many severe sunburns early in life, and long term daily sun exposure (Medline Plus, 2012). Individuals with light colored skin, hair, and eyes have poor tanning abilities and are more likely to have sun-damaged skin (Roewart-Hober, 2007). Radiation therapy in childhood for ringworm on a 58 year old patient caused an aggressively growing BCC that took over most of the posterior scalp (Asilian, 2005). Genetics also contribute to your likelihood of getting a BCC. A family history of skin cancer can increase your chances of having a BCC (Skelton, 2009). Also, there is several inherited and acquired skin disorders associated with BCC. These disorders include xeroderma pigmentosum, nevoid basal cell syndrome, Bazex-syndrome, Rasmussen syndrome, Rombo syndrome, and albinism (Roewert-Hober, 2007). Although there are several contributing factors to BCC, the number one cause is sun exposure and other ultraviolet…
It is similar to scleroderma and scleromyxedema but on distinct difference, NSF is caused by the exposure to gadolinium when patients with renal insufficiently are given gadolinium contrast for a MRI. Patients with NSF most likely develop large patches on the indurated skin with fibrotic nodules and plaques. Some patients develop flexion contractures with accompanying limitation of range of motion. NSF resembles scleromxedema in that it manifests with a proliferation of dermal fibroblasts and dendritic cells, thickened collagen bundles, increased elastic fibers and mucin deposition. This disease is not more common in people with a particular race sex or age. NSF has been reported equally among all age groups and ethnic…
There are several different blood disorders that an individual may experience in their lifetime. Blood disorders are diagnosed by family medical history, symptoms that the individual may be experiencing and the individual’s lifestyle. The three scenarios provided each blood disorder is very different. Amy has iron deficiency anemia whereas, Marcus has sickle cell trait-anemia and Richard is dealing with Thrombocytopenia. Amy, Marcus and Richard have all been diagnosed with a blood disorder where treatments are available. There is information provided for each disorders cause, the criteria for diagnosis, the treatment and how it can be prevented.…