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There are three main types of Pfeiffer syndrome: type I is the mildest and most common; type II is the most severe, with neurological problems and a cloverleaf deformity; and type III is similar to type II, but without the cloverleaf deformity.
Crouzon syndrome is an autosomal dominant genetic disorder known as a branchial arch syndrome. Specifically, this syndrome affects the first branchial (or pharyngeal) arch, which is the precursor of the maxilla and mandible. Because the branchial arches are important developmental features in a growing embryo, disturbances in their development ...
Cardiocranial syndrome, Pfeiffer type is a rare multiple disorder syndrome characterized by congenital heart defects, sagittal craniosynostosis, and severe developmental delay. The condition has been reported in less than 10 patients worldwide. Signs and symptoms. Features of this condition include: Abnormal heart morphology
Carpenter syndrome. Carpenter syndrome, also called acrocephalopolysyndactyly type II, [1] is an extremely rare autosomal recessive [2] congenital disorder characterized by craniofacial malformations, obesity, syndactyly, and polydactyly. [2] Acrocephalopolysyndactyly is a variation of acrocephalosyndactyly that presents with polydactyly.
Pfeiffer’s ongoing series “Four Horsemen of the Apocalypse” confronts the often fleeting fame of top-level sports stars, in carefully-edited photographs.
Infectious mononucleosis ( IM, mono ), also known as glandular fever, is an infection usually caused by the Epstein–Barr virus (EBV). [2] [3] Most people are infected by the virus as children, when the disease produces few or no symptoms. [2] In young adults, the disease often results in fever, sore throat, enlarged lymph nodes in the neck ...
Michelle Pfeiffer, 65, was absolutely radiant in her latest no-makeup Instagram selfie. The Ant Man star was nearly unrecognizable, and held up her adorable new puppy, Dot, in the frame.
Michelle Pfieffer, 65, looked completely unrecognizable in her latest Instagram post. The star sticks to a simple skincare routine and clean beauty products.
Antley–Bixler syndrome. Antley–Bixler syndrome has an autosomal recessive pattern of inheritance. Antley–Bixler syndrome is a rare, severe autosomal recessive [2] congenital disorder characterized by malformations and deformities affecting the majority of the skeleton and other areas of the body. [citation needed]
type I – Apert syndrome; type II – Crouzon syndrome; type III – Saethre–Chotzen syndrome. Robinow-Sorauf syndrome suggested to be included in Saethre-Chotzen classification ; type IV – Mohr syndrome (archaic) type V – Pfeiffer syndrome. Noack syndrome incorporated into Pfeiffer syndrome classification
