peutz–jeghers syndrome in a sentence

• peutz-jeghers综合征    1954年Bruwer等首次使用Peutz-Jeghers综合征这一名称。 1954年开始使用“Peutz-Jeghers综合征”这一名称。 Peutz-Jeghers综合征是一种常染色体显性遗传性疾病，在胃，小肠和结肠内发生多发性错构瘤性息肉。 Peutz-Jeghers综合征(Peutz-Jeghers’s syndrome，下简称为PJS)又称家族性黏膜皮肤色素沉着胃...
• jeghers syndrome    Peutz Jeghers syndrome is rare and studies typically include only a small number of patients. Follow-up care should be supervised by a physician familiar with Peutz Jeghers syndrome. Peu...
• orbital floor syndrome dejean syndrome    Orbital floor syndrome dejean syndrome
• redundant acronym syndrome syndrome    These phases expand to " automated teller machine machine ", " human immunodeficiency virus virus ", " personal identification number number ", and " redundant array of independent disks a...
• syndrome syndrome    These phases expand to " automated teller machine machine ", " human immunodeficiency virus virus ", " personal identification number number ", and " redundant array of independent disks a...
• frits peutz    The city's best known architect is without doubt Frits Peutz. It was designed by Frits Peutz ( best known for the Glaspaleis ) and J . Bongaerts. In the 20th century, architect Frits Peutz...
• jeghers    Peutz Jeghers syndrome is rare and studies typically include only a small number of patients. Follow-up care should be supervised by a physician familiar with Peutz Jeghers syndrome. Peu...
• peutz    The city's best known architect is without doubt Frits Peutz. It is one of the biggest buildings designed by Peutz. It was designed by Frits Peutz ( best known for the Glaspaleis ) and J ....
• 13q deletion syndrome    Congenital heart disease is associated with 13q deletion syndrome. Other skeletal malformations are found with 13q deletion syndrome, including syndactyly, clubfoot, clinodactyly, and malf...
• 1p36 deletion syndrome    There have also been reports of patients with 1p36 deletion syndrome whose parents have a balanced or symmetrical translocation. 1p36 Deletion Syndrome is a congenital genetic disorder cau...
• 22q11 deletion syndrome    "' 22q11 Deletion Syndrome "'is a rare condition which occurs in approximately 1 in 4000 births. Children with schizophrenia have an increase in genetic deletions or duplication mutations ...
• 22q13 deletion syndrome    There is disagreement among researchers as to the exact definition of 22q13 deletion syndrome. Table of protein coding genes involved in 22q13 deletion syndrome ( based on Human Genome Bro...
• 2q37 deletion syndrome    Deletion of GPR35 gene may be responsible for brachydactyly mental retardation syndrome and is mutated in 2q37 monosomy and 2q37 deletion syndrome.
• 3c syndrome    Some immunodeficiency has also been reported in connection with 3C syndrome. It is distinguished from 3C syndrome by differences in facial dysmorphisms. Aortic stenosis and pulmonary steno...
• 3q29 microdeletion syndrome    The clinical phenotype of 3q29 microdeletion syndrome is variable. "' 3q29 microdeletion syndrome "'is a rare genetic disorder resulting from the deletion of a segment of chromosome 3.
• 9q34 deletion syndrome    However, in recent studies, 9q34 deletion syndrome occurs when the EHMT1 gene is non-functioning, as opposed to strictly deletion.
• a syndrome    This is referred to as'complex craniosynostosis'and is typically part of a syndrome. Marin argues that apathy should be regarded as a syndrome or illness. It can also be part of a syndrome...
• aarskog syndrome    Other genetic syndromes occasionally associated with widow's peaks include Waardenburg syndrome and Aarskog syndrome. Many syndromes are associated with clinodactyly, including Down Syndro...
• aase smith syndrome    The condition known as Aase Smith syndrome is named for Smith and colleague Jon Morton Aase.
• aase syndrome    "' Aase syndrome "'or "'Aase Smith syndrome "'is a rare inherited disorder characterized by anemia with some joint and recessive inherited disorder.
• abandoned child syndrome    It is not uncommon for a child to develop abandoned child syndrome due to the parents passing. The ones I can understand a little & ndash; Parricide, Abandoned child syndrome, et al . & nd...
• abcd syndrome    The characteristics of ABCD syndrome are clearly evident in an inflicted individual. Scientists completed a molecular analysis with DNA strands of the patients diagnosed with ABCD syndrome...
• abdallat davis farrage syndrome    He participated in the discovery of Abdallat Davis Farrage syndrome in 1980.
• abdominal compartment syndrome    Abdominal compartment syndrome with visceral hypoperfusion is associated with severe burns of the abdomen and torso. The third is abdominal compartment syndrome that has been reported anyw...
• abdominal syndrome    Speculation on several questions concerning treatment of acute abdominal syndrome with traditional chinese medicine combined with western medicine