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Autosomal dominant multiple pterygium syndrome is a cutaneous condition inherited in an autosomal dominant fashion. [2] Society
Hypoplastic left heart syndrome; Infantile polycystic kidney disease; Iniencephaly; Intracranial teratoma; Intrauterine growth retardation; Klippel–Trénaunay syndrome; Limb body wall complex; Macrosomia; Meconium cyst; Meconium ileus; Microcephaly; Multicystic dysplastic kidney; Multiple pterygium syndrome; Oligohydramnios; Omphalocele ...
Bartsocas-Papas syndrome is a form of popliteal pterygium syndrome and is a very rare disease characterized by congenital craniofacial anomalies, popliteal webbing, and genitourinary and musculoskeletal anomalies. It was first described by Dr. Christos Bartsocas and is more specifically an autosomal recessive popliteal pterygium syndrome. [8]
Multiple organ failure; Multiple pterygium syndrome lethal type; Multiple pterygium syndrome; Multiple s – Multiple v. Multiple sclerosis ichthyosis factor VIII deficiency; Multiple sclerosis; Multiple subcutaneous angiolipomas; Multiple sulfatase deficiency; Multiple synostoses syndrome 1; Multiple system atrophy; Multiple vertebral ...
Mitochondrial myopathy–encephalopathy–lactic acidosis–stroke syndrome; Multiple lentigines syndrome (cardiocutaneous syndrome, Gorlin syndrome II, lentiginosis profusa syndrome, LEOPARD syndrome, progressive cardiomyopathic lentiginosis) Multiple pterygium syndrome; Multiple sulfatase deficiency (Austin disease, mucosulfatidosis)
Neurological conditions, including Parkinson's disease, stroke, multiple sclerosis or amyotrophic lateral sclerosis (ALS), can interfere with the nerves and muscles that control swallowing.
Autosomal dominant multiple pterygium syndrome; B. Bannayan–Riley–Ruvalcaba syndrome; Barakat syndrome; Bardet–Biedl syndrome; Barraquer–Simons syndrome;
Irritable bowel syndrome, or IBS, is among the most common gastrointestinal conditions today. It affects some 10% to 15% of people in the U.S., per the American College of Gastroenterology. A ...