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* Congenital anomaly, popularly referred to as a birth defect, a disorder present at birth, the result of an inherited gene mutation, an error during morphogenesis or fetal development, or an environmental factor
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Congenital and anomaly
Congenital apical displacement of the tricuspid valve is called Ebstein's anomaly and typically causes significant tricuspid regurgitation.
*** Congenital vertebral anomaly, any of several malformations of the spine in animals and infants
Congenital anomaly of the genitalia is a medical term referring to any physical abnormality of the male or female internal or external genitalia present at birth.
Congenital and referred
Disorders referred to as " Congenital Central Hypoventilation Syndrome " or " CCHS " and " Rapid-Onset Obesity, Hypothalamic Dysfunction, Hypoventilation, with Autonomic Dysregulation " or ROHHAD are recognized.
Congenital and birth
Congenital heart defects are defects in the structure of the heart which are present at birth.
# Congenital: Children of a healthy mother can, very rarely, develop myasthenic symptoms beginning at birth, congenital myasthenic syndrome or CMS.
* Congenital nevus: Small to large nevus present at or near time of birth.
Cytomegalovirus ( Congenital )-one group of herpes viruses that infects humans and can cause a variety of clinical symptoms, including deafness or hearing impairment ; infection with the virus may be either before or after birth.
* Congenital defect – problems or conditions that are present at birth.
* Congenital variant ( Rolando variant ): in this severe subtype of Rett syndrome, the development of the patients and their head circumference are abnormal from birth.
* Congenital lactase deficiency is a very rare, autosomal recessive genetic disorder that prevents lactase expression from birth.
Congenital lactase deficiency ( CLD ), where the production of lactase is inhibited from birth, can be dangerous in any society because of infants ' nutritional reliance on breast milk during their first months.
The absence of the sense of smell from birth is called Congenital Anosmia.
* Congenital disorder, a medical condition present at birth
Congenital melanocytic nevus is a type of melanocytic nevus ( or mole ) found in infants at birth.
Congenital hypothyroidism ( CH ) is a condition of thyroid hormone deficiency present at birth.
Congenital heart disease is any disease due to an inborn defect in the heart that is present at birth.
* Congenital problems ( defects present at birth ) affecting the heart and lungs ( 48 %);
* Congenital nevus implying a melanocytic nevus present at birth or near birth.
Congenital syphilis is syphilis present in utero and at birth, and occurs when a child is born to a mother with secondary syphilis.
* Congenital muscular dystrophy, a form of muscular dystrophy that is present from birth
* Congenital ( present from birth )
Congenital hypertrichosis is always present at birth.
Congenital hypertrichosis lanuginosa is noticeable at birth, with the infant completely covered in thin lanugo hair.
Congenital diaphragmatic hernia ( CDH ) is a congenital malformation ( birth defect ) of the diaphragm.
Congenital and defect
# REDIRECT Congenital heart defect
# REDIRECT Congenital heart defect
; Congenital heart defect correction: Percutaneous approaches can be employed to correct atrial septal and ventricular septal defects, closure of a patent ductus arteriosus, and angioplasty of the great vessels.
Congenital adrenal hyperplasia due to 17α-hydroxylase deficiency is an uncommon form of congenital adrenal hyperplasia resulting from a defect in the gene CYP17A1, which encodes for the enzyme 17α-hydroxylase.
# REDIRECT Congenital heart defect
# REDIRECT Congenital heart defect
# REDIRECT Congenital heart defect
* Congenital heart defect, a defect in the structure of the heart and great vessels which is present at birth
Congenital and disorder
# redirect Congenital disorder
* Congenital chloride diarrhea, a rare disorder in babies
In May 2008, three groups reported positive results using gene therapy to treat Leber's Congenital Amaurosis ( LCA ), a rare inherited retinal degenerative disorder that causes blindness in children.
* Congenital myasthenic syndrome, An inherited neuromuscular disorder
# REDIRECT Congenital disorder of glycosylation
Congenital disorder -
# redirect Congenital disorder
# REDIRECT Congenital disorder
* Congenital disorder of glycosylation also known as " CDG Syndrome "
Congenital amegakaryocytic thrombocytopenia ( CAMT ) is a rare inherited disorder.
* Congenital diaphragmatic hernia, a disorder involving abnormal development of the diaphragm
# REDIRECT Congenital disorder
# REDIRECT Congenital disorder
# REDIRECT Congenital disorder
Amniotic band syndrome ( also known as " ADAM complex ", " Amniotic band sequence ", " Congenital constriction bands " and " Pseudoainhum ") is a congenital disorder caused by entrapment of fetal parts ( usually a limb or digits ) in fibrous amniotic bands while in utero.
# REDIRECT Congenital disorder
Congenital insensitivity to pain with anhidrosis ( CIPA ), also called hereditary sensory and autonomic neuropathy type IV — is an extremely rare inherited disorder of the nervous system which prevents the sensation of pain, heat, cold, or any real nerve-related sensations ( including feeling the need to urinate ); however, patients can still feel pressure.
* Congenital insensitivity to pain with anhidrosis ( HSAN Type IV ), a rare neural disorder, in which the patient does not feel pain, heat or cold.
Congenital stationary night blindness is also an opthalmologic disorder in horses with leopard spotting patterns, such as the Appaloosa.
* Congenital or acquired ( coagulation disorder
# redirect Congenital disorder
# REDIRECT Congenital disorder
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