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Congenital adrenal hyperplasia (CAH) Congenital central hypoventilation syndrome; Congenital diaphragmatic hernia (CDH) Congenital Disorder of Glycosylation (CDG) Congenital hyperinsulinism; Congenital insensitivity to pain with anhidrosis (CIPA) Congenital pulmonary airway malformation (CPAM) Conjoined twins; Costello syndrome; Craniopagus ...
Lesch–Nyhan syndrome; Lethal congenital contracture syndrome; Lethal white syndrome; Leukotriene receptor antagonist-associated Churg–Strauss syndrome; Levator ani syndrome; Leydig cell hypoplasia; Liddle's syndrome; Liebenberg syndrome; LIG4 syndrome; Lima syndrome; Limb girdle syndrome; Limber tail syndrome; Limb–mammary syndrome ...
Hemolytic–uremic syndrome: Horner's Syndrome Triad: ptosis (eyelid), miosis, anhydrosis: Horner's syndrome: Hutchinson's triad: Hutchison's teeth, Interstitial keratitis, Nerve deafness: Congenital syphilis: Kartagener Syndrome Triad: Triad of bronchiectasis, Recurrent sinusitis, and, Situs inversus, Kartagener syndrome: Leriche's syndrome Triad
A congenital malformation is a physical anomaly that is deleterious, i.e. a structural defect perceived as a problem. A typical combination of malformations affecting more than one body part is referred to as a malformation syndrome. [citation needed] Some conditions are due to abnormal tissue development:
respiratory distress syndrome; measles; meconium aspiration syndrome; metapneumovirus (hMPV) infection; necrotizing enterocolitis; neonatal conjunctivitis; parainfluenza (PIV) infection; pertussis; poliomyelitis; prenatal Listeria; Group B streptoccus infection; Tay–Sachs disease; tetanus; Ureaplasma urealyticum infection; respiratory ...
Congenital heart disease refers to heart problems that you’re born with, like holes in the heart, malformed valves, and others. Some examples of congenital heart disease include : Pulmonary ...
Around the world, the most common cause of congenital iodine deficiency syndrome (endemic cretinism) [1] is dietary iodine deficiency. Iodine is an essential trace element, necessary for the synthesis of thyroid hormones. Iodine deficiency is the most common preventable cause of neonatal and childhood brain damage worldwide. [11]
The following is a list of genetic disorders and if known, type of mutation and for the chromosome involved. Although the parlance "disease-causing gene" is common, it is the occurrence of an abnormality in the parents that causes the impairment to develop within the child. There are over 6,000 known genetic disorders in humans.