Search results
Results From The WOW.Com Content Network
Saethre–Chotzen syndrome ( SCS ), also known as acrocephalosyndactyly type III, is a rare congenital disorder associated with craniosynostosis (premature closure of one or more of the sutures between the bones of the skull ). This affects the shape of the head and face, resulting in a cone-shaped head and an asymmetrical face.
Ectodermal dysplasia. A patient displaying peg-shaped teeth and sparse hair characteristic of ectodermal dysplasia. Specialty. Medical genetics. Ectodermal dysplasia ( ED) is a group of genetic syndromes all deriving from abnormalities of the ectodermal structures. [1] : 570 More than 150 different syndromes have been identified.
An affected child can be treated using antibiotics much like an adult; however, any developmental symptoms are likely to be permanent. [32] The greater the duration between the infection of the mother and conception , the better the outcome for the infant including less chance of stillbirth or developing congenital syphilis.
The following article is a summary of notable incidents at the amusement parks and water parks that are operated by Six Flags Entertainment Corporation.In some cases, these incidents occurred while the park was under different management or ownership.
The Baby Tooth Survey was initiated by the Greater St. Louis Citizens' Committee for Nuclear Information in conjunction with Saint Louis University and the Washington University School of Dental Medicine as a means of determining the effects of nuclear fallout in the human anatomy by examining the levels of radioactive material absorbed into the deciduous teeth of children.
Nance–Horan syndrome is a rare X-linked dominant syndrome characterized by congenital cataracts leading to profound vision loss, characteristic dysmorphic features, and dental anomalies. [1] [2] Microcornea, microphthalmia, and mild or moderate intellectual disability may accompany these features. Heterozygous females often manifest similarly ...
According to Dr. Nicole Alicia Sparks, a board-certified OB/GYN, two hormones that increase during pregnancy are responsible for swollen body parts, including the nose. “There are so many ...
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.