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What is congenital heart disease?

Congenital heart disease is a malformation of the heart or adjacent blood vessels present in the newborn or fetus. It should be noted that some heart diseases manifest themselves months or years later.

In this case, we are talking about a birth problem in which the heart has congenital disabilities, such as an incomplete heart, with narrow blood vessels, leaky valves, or holes in the septa…

There are different types of congenital heart imperfections, some of which are mild and only pose a slight risk to the child’s health, and others may require immediate surgery.

Heart disease can be classified into:

  1. Heart disease that obstructs blood flow
  2. Cyanotic congenital heart disease, in which abnormal blood flow is from the pulmonary to the systemic circulation, passing deoxygenated blood to organs and tissues
  3. Those that produce short circuits between left and right (the passage of blood from the systemic to the pulmonary circulation are the interventricular communications and the interatrial communications).
  • Ventricular communication: they have a hole that communicates both ventricles, the most frequent congenital heart disease. It may be sarcoidosis, and the gap may close on its own, but if it continues to grow, excessive blood will be pumped into the lungs, leading to heart failure.
  • An atrial septal defect is a hole between the atria that allows blood to pass between them. The blood will fluctuate between the left and the right, and if too much blood reaches the right, the lungs will be pressed. Usually, atrial septal defects do not cause problems, although sometimes they cause too much, such as heart failure, hypertension, strokes…
  • Tetralogy of Fallot: this is a complex heart disease in which interventricular communication, pulmonary artery stenosis, right ventricular hypertrophy, and dominance of the aorta stand out. The baby takes on a sickly blue or purple hue. It prevents blood from getting the lungs to be oxygenated.  Advances in new surgical techniques allow these problems to be corrected.
  • Long QT syndrome: This is a structural abnormality in the potassium and sodium channels of the heart. It can cause arrhythmias that lead to syncope, seizures, stops, and even sudden death.
  • Short QT syndrome: this is a genetic syndrome related to the presence of atrial fibrillation. It is characterized by having an electrocardiogram QT interval faster than expected.
  • Brugada syndrome: this is a genetic disease characterized by the presence of an electrocardiographic abnormality. It is a hereditary disease.

These cardiac disorders are related to sudden death diseases.

Medical tests for congenital heart disease

Most congenital heart diseases are diagnosed by ultrasound before delivery occurs in routine studies performed on pregnant women to monitor the progress of pregnancy and the health status of both the mother and the fetus.

There are heart diseases that are detected only at birth or shortly after. If there are congenital severe heart diseases, these will be identified in the baby’s check-ups after birth.

Prognosis of congenital heart disease

As mentioned in the previous section, there are numerous congenital heart diseases whose severity varies, from practically invisible problems that are resolved spontaneously over time to severe conditions in which the patient will require hospital admission and surgery. Practically urgent.

Causes of congenital heart disease

The causes of congenital heart disease are unidentified, although some factors have been identified that can increase these diseases:

  • Genetic cause: they can be part of genetic or chromosomal syndromes such as Down syndrome, Marfan syndrome, Noonan syndrome, or Turner syndrome.
  • Nutritional status of the mother: lack of iodine, folate, being overweight, or diseases such as diabetes are related to the appearance of congenital anomalies in the fetus, according to the World Health Organization.
  • Infections and toxic substances: the consumption of alcoholic beverages or tobacco, some medicines or chemical substances, and even diseases such as rubella can favor the appearance of heart disease.

Can congenital heart disease be prevented?

Primary prevention measures for congenital malformations can reduce the frequency with which these problems appear.

  • Improve the diet of pregnant women with vitamins and minerals, such as folic acid
  • Eliminate tobacco and alcohol consumption in pregnant women
  • Control blood glucose levels if the pregnant woman suffers from diabetes
  • Avoid exposure to toxic substances

Congenital heart disease treatments

  • Pharmacological treatment: it occurs in the acute phase when the patient has suffered angina pectoris or heart attack. It is a heart attack due to total occlusion of the artery, and an attempt is made to unclog it. The medication used is acetylsalicylic acid (aspirin), platelet antiaggregants, anticoagulants, beta-blockers, nitroglycerin, thrombolytics or fibrinolytic, and drugs to prevent pain.
  • Surgical treatment: occurs in severe problems or when medication is insufficient. Surgery is performed on the artery. Percutaneous angioplasty or revascularization, coronary artery bypass surgery, or bypass.
  • Long-term treatment: consists of modifying the patient’s lifestyle. Quit smoking, moderate alcohol consumption, balanced diet, regular exercise, control risk factors, and relax.

What specialist treats congenital heart disease?

Babies or children with congenital problems are diagnosed and treated by a pediatric cardiologist. If an intervention is necessary, the one in charge of dealing with the disease will be the cardiac surgeon or the cardiovascular surgeon.

Heart disease can have different levels of severity and a wide variety of symptoms. Mild heart disease can become asymptomatic, and a serious one that may be latent can appear suddenly.

seborrheic dermatitis

Seborrheic dermatitis is a papulosquamous dermatosis that is very common, chronic, and relapsing, easy to diagnose, which settles preferentially in the areas with the highest density of sebaceous glands face, scalp, presternal area, and folds. It has a typical clinic, easily recognizable: pink erythema and yellowish-white scaling. It presents tremendous variability in the inter-individual severity and even in individuals throughout his life. It is shown in neonates and adults and has various forms. Its pathogenesis is still uncertain, involving several factors (seborrhea, microbiological effects, neurological factors, etc.). Even though the family association is appreciated, a relationship has not been confirmed form of inheritance

Who gets Seborrheic Dermatitis?

Seborrheic dermatitis occurs in infants under three months and usually gets better between 6 and 12 months.

Adult seborrheic dermatitis appears in late adolescence. Its prevalence is more in young and older adults. It is more common in men than in women. The following factors may be associated with severe seborrheic dermatitis in adults:

  • Oily skin (seborrheic illness)
  • A familial propensity for a family history of seborrheic dermatitis or psoriasis
  • Immunosuppression: Organ transplant recipients, patients with human immunodeficiency virus (HIV) infection, and lymphoma
  • Neurological and psychiatric disorders: Congenital disorders such as Parkinson’s disease, late-onset motor disorders, depression, epilepsy, facial paralysis, spinal cord injury, and Down’s disease
  • Treatment of psoriasis with psoralen and ultraviolet A (PUVA) therapy.
  • Sleep deprivation and stressful events.

What chances do people with seborrheic dermatitis have?

Seborrheic dermatitis is a chronic state, so you may have to deal with it at some point in your life. They can go through long periods with few or no symptoms. You will also experience flare-ups, episodes where symptoms become more severe.

Over time, you can find a skincare routine that works for you and lessens the effects of the condition. Recognizing and eliminating stimuli can also help you effectively manage seborrheic dermatitis. It does not lead to severe medical conditions or other complications.

The flat cap usually disappears within six months without treatment.

Etiopathogenesis

It is not known; several factors likely contribute to their development.

Seborrhea

The lesions are located in areas with a high density of pilosebaceous units of the face, scalp, and torso, and patients often have oily skin. However, not all affected patients have increased sebum production. Seborrheic dermatitis is neither a disease of the sebaceous glands nor does it occur

GOOD POINT

Concept. Seborrheic dermatitis is a chronic entity, recurrent, affecting areas of the body with an increased density of sebaceous glands. There are two different clinical forms, infantile seborrheic dermatitis, which occurs in all three.

First months of life and seborrheic dermatitis in adults.

Pathogens

Its pathogenesis remains uncertain. Involves many factors. Unlike newborns, there is no relationship between

increased sebum production and seborrheic dermatitis. The role of Malassezia furfur in sick. Affected patients may have an altered immune response to the micro-organism, which justifies its dermatitis.

Diagnosis

Diagnosis is based on clinical manifestations, which have very high typical and easily identifiable, with peculiarities depending on the age and location of the lesions. Well-established factors include temperature differences, drugs, neurological diseases, and situations suppressing immunity. The primary differential diagnosis in children is atopic dermatitis; it varies depending on the affected part of the body in adults. Sometimes, especially on the scalp, the difference

in psoriasis, it is impossible; many authors refer to these clinical forms as seborrhea.

Therapy

While it is self-sufficient in newborns, it is a chronic and recurrent disease in adults. In most cases, it is a prophylactic maintenance treatment. In this sense, besides the classic ready-made antifungals that label subjects with immunomodulators, we may have vigorous anti-inflammatory activity without the side effects of long-term use of corticosteroids.