「Congenital」の共起表現一覧(1語右で並び替え)
該当件数 : 264件
| Calves suffer from few | congenital abnormalities but the Akabane virus is widel |
| Congenital abnormalities and childhood cancer | |
| abortions, stillbirths, premature births and | congenital abnormalities, but occurs only during some y |
| eyes, deformities, tumors, cleft lip/palate, | congenital abnormalities, burns & leprosy, oral disease |
| ch primarily dealt with genetic diseases and | congenital abnormalities. |
| n its dorsal fin instead of the normal 10, a | congenital abnormality known to occasionally occur in g |
| also bifurcated rib or sternum bifidum) is a | congenital abnormality of the rib cage and associated m |
| The most common | congenital abnormality of the heart is the bicuspid aor |
| In the severest form of | congenital adrenal hyperplasia, complete masculinizatio |
| Congenital adrenal hyperplasia (CAH) refers to any of s | |
| Mutations in the gene for StAR cause lipoid | congenital adrenal hyperplasia (lipoid CAH), in which p |
| He also delineated forms of | congenital adrenal hyperplasia. |
| useful in the diagnosis of certain forms of | congenital adrenal hyperplasia. |
| tations in this gene result in both X-linked | congenital adrenal hypoplasia and hypogonadotropic hypo |
| In patients with | congenital adrenal hyperplasia due to 3 beta-hydroxyste |
| People with | congenital adrenal hyperplasia may also undergo this to |
| Rarer causes include precocious puberty, | congenital adrenal hyperplasia, and androgen-producing |
| relatively rare, it is the third most common | congenital airway problem (after laryngomalacia and voc |
| n documented in cases of autosomal recessive | congenital alopecia and atrichia with papular lesions. |
| h T-cell immunodeficiency, the skin disorder | congenital alopecia, and nail dystrophy. |
| iated with photoreceptor degeneration, Leber | congenital amaurosis type III and the autosomal dominan |
| Born with Leber's | congenital amaurosis, Tan worked as a street busker for |
| Other cone diseases such as Leber's | congenital amaurosis, cone-rod dystrophy, and certain t |
| disease, choroideremia, retinoschisis, Leber | congenital amaurosis, Bardet-Biedl syndrome, cone dystr |
| percent field of vision, both due to Leber's | congenital amaurosis. |
| t of two of three test patients with Leber's | congenital amaurosis. |
| Up to 50% of cases have other | congenital anomalies including cleft lip, cleft palate, |
| ed "there appears to be no increased risk of | congenital anomalies, altered sex ratio, or early pregn |
| e or preauricular tag is a relatively common | congenital anomaly of the first branchial arch. |
| portant anatomic landmark for pathology in a | congenital anomaly known as posterior urethral valves, |
| A Type I Arnold-Chiari malformation is a | congenital anomaly of the brain in which the cerebellar |
| Cryptophthalmos is a rare | congenital anomaly in which the skin is continuous over |
| peration in England for 'hole-in-the-heart' ( | congenital atrial septal defect) was performed at Birmi |
| ture generations than would parents having a | congenital bias towards the production of females. |
| ral anophthalmia with pterygium syndrome and | congenital bilateral hip dysplasia. |
| First, inbreeding does not directly lead to | congenital birth defects per se; it leads to an increas |
| A homozygote encoding a | congenital birth defect will produce children with birt |
| ce of the taboo would lower the incidence of | congenital birth defects caused by inbreeding. |
| platelet alpha-granule deficiency, is a rare | congenital bleeding disorder caused by a reduction or a |
| with people in early childhood: The case of | congenital blindness. |
| Eiesland, born with a | congenital bone defect, underwent numerous operations i |
| Dandy Walker malformation is a | congenital brain malformation that is characterized by |
| The common cause is | congenital, but it can also be caused by maternal stero |
| In 2001, he was named chief of pediatric and | congenital cardiac surgery at the Arkansas Children's H |
| The Atlas of | Congenital Cardiac Disease |
| tions in this gene have been associated with | congenital chloride diarrhoea , a treatable disease. |
| s congenita (also known as "Cutis aplasia," " | Congenital absence of skin," and "Congenital scars") is |
| x in infants) may be a tool in detecting the | congenital clapsed thumb early in infancy. |
| Although | congenital, CM can also be induced due to physical head |
| mary Biggs and Ethel Bidwell, to investigate | congenital coagulation defects, the treatment of bleedi |
| the perfect penis, Majors has Hypospadias, a | congenital condition he says makes him 'technically int |
| Wilson-Turner syndrome is a | congenital condition characterized by mental retardatio |
| confirmed that his aneurysm was caused by a | congenital condition and that it wasn't triggered by an |
| tary about Kenny's adaptation to his unusual | congenital condition, the absence of his pelvis and leg |
| It may be either an acquired or a | congenital condition. |
| 's Medical Research Institute, which studies | congenital conditions such as cancer, epilepsy and birt |
| d often relying on unique genetic traits and | congenital conditions. |
| Arterial tortuosity syndrome is a rare | congenital connective tissue condition disorder charact |
| Lethal | congenital contracture syndrome 1 (LCCS1), also called |
| , as in other communities with high rates of | congenital deafness such as Martha's Vineyard. |
| s a syndrome characterized by choroideremia, | congenital deafness and obesity. |
| ation, legg-calve-perthes, thyroid, cardiac, | congenital deafness, sebaceous adenitis, and shoulder O |
| ncreased risk of ventricular arrhythmias and | congenital deafness. |
| mals, such as white cats, have a tendency to | congenital deafness. |
| s (also called paraomphalocele) represents a | congenital defect characterized by a defect in the ante |
| This is a | congenital defect which consists of bilateral amputatio |
| Jeff's | congenital defect hasn't prevented him from great achie |
| Gastroschisis as a stand-alone | congenital defect is usually inherited in an autosomal |
| ceiving a child with a hereditary disease or | congenital defect. |
| abilitation of those with limb amputation or | congenital deficiency, and those with neurological disa |
| treated patients with tuberculosis, rickets, | congenital deformities and poliomyelitis. |
| Anotia ("no ear") describes a rare, | congenital deformity, a missing auricle, the external, |
| ad her leg amputated below the knee due to a | congenital deformity. |
| me is a cutaneous condition characterized by | congenital dermatoglyph malformations. |
| perplastic primary vitreous (PHPV) is a rare | congenital developmental anomaly of the eye that result |
| intains that the child will not be born with | congenital disabilities, a statement that is later foun |
| st Yorkshire and was the first person with a | congenital disability - Osteogenesis imperfecta (brittl |
| Menkes disease is a | congenital disease that is a cause of copper deficiency |
| Microcoria is a | congenital disease in which the pupils of the subject a |
| atotic poikiloderma of Kindler and Weary,", " | Congenital poikiloderma with blisters and keratoses," " |
| Its symptoms include hypermobility, | congenital dislocations, brachycephaly and cleft palate |
| Fountain syndrome is an autosomal recessive | congenital disorder characterized by mental retardation |
| Kelly syndrome is a rare autosomal dominant | congenital disorder consisting of radial hypoplasia, tr |
| Young Simpson syndrome (YSS), is a rare | congenital disorder with symptoms including hypothyroid |
| fects in this gene have been associated with | congenital disorder of glycosylation type Id (CDG-Id) c |
| An imperforate lacrimal punctum is a | congenital disorder of dogs involving the lack of an op |
| ilayered patellae, is an autosomal recessive | congenital disorder affecting cartilage and bone develo |
| led Cleidocranial dysplasia, is a hereditary | congenital disorder due to haploinsufficiency caused by |
| facial expression, is an autosomal recessive | congenital disorder characterized by inverted facial ex |
| brofacial syndrome is an autosomal recessive | congenital disorder characterized by mental retardation |
| tremely rare autosomal recessive multisystem | congenital disorder which affects the skeletal system, |
| Congenital disorder of glycosylation type IIc or Leukoc | |
| Myelokathexis is a | congenital disorder of the white blood cells that cause |
| etimes fatal autosomal recessive multisystem | congenital disorder featuring abnormal development of t |
| nova syndrome, is a rare autosomal recessive | congenital disorder causing chromosomal instability, pr |
| , is a rare, very severe autosomal recessive | congenital disorder characterized by malformations and |
| gital changes, is a rare autosomal recessive | congenital disorder first reported in 1939 by A. Nakajo |
| wall Syndrome) is a rare autosomal recessive | congenital disorder characterized by growth failure, im |
| rpus callosum, is a rare autosomal recessive | congenital disorder characterized by albinism, agenesis |
| from rape or statutory rape, or if a serious | congenital disorder was detected in the fetus. |
| splastic nails, is a rare autosomal dominant | congenital disorder associated with a range of features |
| Congenital disorder | |
| It is also known as | Congenital disorder of glycosylation 1m. |
| Bangstad syndrome is a severe, inherited | congenital disorder associated with abnormalities of th |
| In the | congenital disorder cleidocranial dysostosis, the anter |
| Defects can be associated with | Congenital disorder of glycosylation type IIc. |
| MORM syndrome is an autosomal recessive | congenital disorder characterized by mental retardation |
| e (LS), is a rare usually autosomal dominant | congenital disorder that occurs in about every 1 in 100 |
| It can also be a | congenital disorder, caused by compression of the nose |
| syndrome, is a very rare autosomal recessive | congenital disorder. |
| ome, is an extremely rare autosomal dominant | congenital disorder. |
| eppen-Lubinsky syndrome is an extremely rare | congenital disorder. |
| llips syndrome is a rare autosomal recessive | congenital disorder. |
| ted with specific granule deficiency, a rare | congenital disorder. |
| r these procedures applied to a neonate with | congenital disorders including Malpuech syndrome regard |
| ‘white'] refers to a heterogeneous group of | congenital disorders in melanin pigment biogenesis. |
| mutation, can be associated with non-genetic | congenital disorders, but has also been observed to be |
| ophoric dysplasia, a typically fatal form of | congenital dwarfism. |
| It is associated with a | congenital dysfunction of the enzyme cystathionase, or |
| The rarest is | Congenital erythropoetic porphyria (C.E.P) otherwise kn |
| Gunther disease, also known as | congenital erythropoietic porphyria (CEP), uroporphyrin |
| There may be | congenital extrinsic compression, commonly by an abnorm |
| hy, including Duchenne, Becker, limb girdle, | congenital, facioscapulohumeral, myotonic, oculopharyng |
| ochondrodysplasia known for a characteristic | congenital feature in which bones of the arms and legs |
| myotubular myopathy, central core myopathy, | congenital fiber type disproportion, and multicore myop |
| Congenital fibrosis of the extraocular muscles, or CFEO | |
| d Gilbert's syndrome, is responsible for the | congenital form of Lucey-Driscoll syndrome. |
| Congenital forms of hyperinsulinemic hypoglycemia can b | |
| Congenital generalized lipodystrophy (also known as Ber | |
| It can be associated with | Congenital generalized lipodystrophy type 2. |
| professionally in Italy after adjusting to a | congenital health condition that temporarily sidetracke |
| h arteries, implicating them as mediators of | congenital heart disease. |
| searcher, author or "Cardiac Development and | Congenital Heart Disease" (2008)--Lawrlafo (talk) 02:39 |
| Swami Prajnanpada had a | congenital heart condition which deteriorated with pass |
| re mental retardation, cleft lip and palate, | congenital heart defects, hypoplastic (underdeveloped) |
| died in January 2009 aged 8 months due to a | congenital heart defect. |
| sbyterian Medical Center, and specializes in | congenital heart disease. |
| mplantation, the first successful bypass for | congenital heart defect and the first laser angioplasty |
| 47% of babies born with Down's Syndrome have | congenital heart defects, but with today's advances in |
| order, delayed growth and motor development, | congenital heart disease, genitourinary anomalies and a |
| with abnormalities in the bones of the legs, | congenital heart defects and craniofacial defects. |
| related to the natural history of different | congenital heart diseases and the results of surgery or |
| In screening for | congenital heart disease in pediatric patients, an NT-p |
| osus," one of many cyanotic heart defects or | congenital heart defects. |
| ience with his daughter, who was born with a | congenital heart defect, and suggested that the life-sa |
| anomalies including post-axial polydactyly, | congenital heart defects (most commonly an atrial septa |
| research, and prevention activities related | congenital heart defects, nervous system malformations |
| ogy, Cardio Vascular surgery, Paediatric and | Congenital Heart surgery under Centre for Heart Disease |
| Malalignment of the septum can cause the | congenital heart condition Tetralogy of Fallot. |
| , Evans died from complications related to a | congenital heart condition. |
| 1948 he pioneered the surgical treatment of | congenital heart disorders in the Soviet Union. |
| He was also a pioneer in research on | congenital heart defects. |
| en hospitalized for three weeks because of a | congenital heart defect. |
| such as The Natural and Unnatural History of | Congenital Heart Disease (2009). |
| Born with several | congenital heart defects, Wright received a heart trans |
| l attempting to increase public awareness of | congenital heart defects. |
| first son, Ted, who was born in 1888 with a | congenital heart defect and feeding problems. |
| and in 1964, gave birth to an infant with a | congenital heart defect. |
| ties of the heart that are present at birth ( | congenital heart defects). |
| e Group has contact with Down's Syndrome and | congenital heart defect groups across the world, many o |
| Minkowski-Chauffard disease: | Congenital hemolytic anemia with spherocytosis, splenom |
| was born in 1958 in the Soviet Union with a | congenital hip defect. |
| cement surgery in early December, 2008 for a | congenital hip problem, but was back competing by late |
| When | congenital hyperinsulinism is due to focal defects of t |
| In more severe cases of persistent | congenital hyperinsulinism unresponsive to drugs, a nea |
| Adults with the mildest degrees of | congenital hyperinsulinism may simply have a decreased |
| beta cells, such as in many of the forms of | congenital hyperinsulinism, and more rarely in adults, |
| as insulinoma (a tumor producing insulin) or | congenital hyperinsulinism. |
| itary disorders characterized by generalized | congenital hypertrichosis. |
| autosomal dominant fashion, characterized by | congenital hypopigmented macules. |
| at Jeffrey Hudson must have been affected by | congenital hypopituitarism, as few known conditions oth |
| Mutations in this gene are associated with | congenital hypothyroidism and cleft palate with thyroid |
| Congenital Ichthyosiform Erythroderma (CIE), also known | |
| s epilepsy, mental retardation, infantilism, | congenital ichthyosis, and retinitis pigmentosa.:502:56 |
| iodystrophy (TTDP), trichothiodystrophy with | congenital ichthyosis, Tay syndrome or sulfur-deficient |
| tions, and Myelokathexis syndrome) is a rare | congenital immunodeficiency disorder characterized by c |
| Some patients have a | congenital inability to synthesize certain enzymes, so |
| Some may cross the placenta and cause | congenital infection of the fetus. |
| Congenital lactase deficiency or CLD is a gastrointesti | |
| a high concentration in Finland suffers from | congenital lactase deficiency. |
| Berardinelli-Seip | congenital lipodystrophy is a rare autosomal recessive |
| ment including early intestinal obstruction, | congenital lung cysts, congenital syphilis, congenital |
| emities distal to the point of constriction ( | congenital lymphedema) |
| rome or Maroteaux-Malamut syndrome is a rare | congenital malformation syndrome which involves shorten |
| ystrophy syndrome) is an autosomal recessive | congenital malformation disorder affecting tissues asso |
| 18q deletion syndrome is a | congenital malformation syndrome characterized by bilat |
| ned additional depth of knowledge concerning | congenital malformations by working in Seattle with the |
| iew studies have found that overall rates of | congenital malformations in infants exposed to lamotrig |
| els, no decrease in fertility or increase in | congenital malformations have been observed. |
| esearch has been far-ranging in the areas of | congenital malformations including neural tube defects, |
| The effects of cancer or | congenital malformations may be too low to assess. |
| umented several cases of individuals who had | congenital malformations of the skull. |
| Many of the | congenital malformations found with Malpuech syndrome c |
| lydactyly, is a complex combination of human | congenital malformations (birth defects). |
| ized in surgery, particularly with regard to | congenital malformations of the uro-genital tract. |
| res grossly) may be used to describe certain | congenital malformations, injuries, surgeons who subspe |
| he post-doctoral level in the areas of human | congenital malformations, carcinogenesis and mutagenesi |
| neurosurgery, and treatment of children with | congenital malformations. |
| e to the presence of developmental delays or | congenital malformations. |
| in antenatal screening of pregnant women for | congenital malformations. |
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