Acrorenal syndrome is a group of disorders associated with malformations of the kidneys and limbs. Acrorenal syndrome exists in affected individuals from birth and is characterized by an autosomal recessive mode of inheritance. Acrorenal syndrome is relatively rare. What is acrorenal syndrome? Acrorenal syndrome is a hereditary condition that results in malformations of the limbs … Acrorenal Syndrome: Causes, Symptoms & Treatment
Poland syndrome is a complex of inhibitory malformations caused by disorders during embryonic development. The leading symptom is the unilateral lack of attachment of parts of the large pectoral muscle. The laterally different breasts can be aligned in a cosmetic correction. What is Poland syndrome? The disease group of congenital malformations contains some malformation syndromes … Poland Syndrome: Causes, Symptoms & Treatment
Oligohydramnios sequence represents the description of the effects of insufficient amniotic fluid production. These are severe malformations that develop due to low amniotic fluid volumes during embryogenesis. The condition is fatal. What is an oligohydramnios sequence? Oligohydramnios sequence refers to the effects of insufficient amniotic fluid production during pregnancy. Due to constricted space because of … Oligohydramnios Sequence: Causes, Symptoms & Treatment
Sirenomelia is a malformation of the lower half of the fetus‘ body, beginning with the pelvic area and ending with the feet. It is also called symmelia, sympodia, or simply mermaid syndrome. The ICD-10 classification is Q47.8. What is sirenomelia? Sirenomelia is characterized by a deformity of the legs and feet. These are, depending on … Sirenomelia: Causes, Symptoms & Treatment
Potter syndrome is a combination of agnesia of both kidneys and a resulting lack of amniotic fluid during pregnancy. Without the amniotic fluid, the fetus is impaired in development and forms, for example, underdeveloped lungs that are incompatible with life. The course of the syndrome is necessarily lethal. What is Potter syndrome? During embryogenesis, cells … Potter Syndrome: Causes, Symptoms & Treatment
Renal agenesis is the absence of embryoanal development of one or both renal anlagen. Unilateral renal agenesias are usually asymptomatic and do not affect life, whereas bilateral forms are usually lethal. In bilateral agenesis, renal transplantation is the only effective therapy. What is renal agenesis? During embryogenesis, kidneys develop piecemeal on a healthy embryo. This … Renal Agenesis: Causes, Symptoms & Treatment
Multicystic kidney dysplasia is a congenital kidney disease, but it is not hereditary. The degree of expression of the disease varies. A cystic kidney forms. What is multicystic kidney dysplasia? Multicystic kidney dysplasia is classified as part of the polycystic kidney disease (PKD) group. However, unlike the classic polycystic kidney diseases, it is not hereditary. … Multicystic Kidney Dysplasia: Causes, Symptoms & Treatment
