Anagrammer & Oplysninger om | engelsk ord PECTUS

Eksempler på brug af PECTUS i en sætning

• Apart from the possible physiologic consequences, pectus malformations can have a significant psychologic impact.
• Lower levels of mRNA expression were associated with a higher risk for ectopia lentis, the displacement of the crystalline lens of the eye, and pectus deformity, an abnormality of the chest muscle, indicating that variation in expression could be due to levels of expressivity and not genotype.
• It is also associated with growth retardation, megaloblastic anemia, pectus excavatum, scoliosis, vomiting, diarrhea, and hepatosplenomegaly.
• Other characteristics that are less frequently seen are: broad nasal base, low anterior hair line, low set ears, crowding of the teeth, maxillary hypoplasia, rounded and sloping shoulders, pectus excavatum, scoliosis, high arched palate, orbital dystopia, low implant of the breasts with asymmetric nipples and volume, webbed neck, hand or foot abnormalities such as clinodactyly (most common is a curved 5th finger) and cutaneous syndactyly (webbed fingers / toes).
• Fitzsimmons–Guilbert syndrome is an extremely rare genetic disease characterized by a slowly progressive spastic paraplegia, skeletal anomalies of the hands and feet with brachydactyly type E, cone-shaped epiphyses, abnormal metaphyseal–phalangeal pattern profile, sternal anomaly (pectus carinatum or excavatum), dysarthria, and mild intellectual deficit.
• Zori–Stalker–Williams syndrome, also known as pectus excavatum, macrocephaly, short stature and dysplastic nails, congenital disorder associated with a range of features such as pectus excavatum, macrocephaly and dysplastic nails, familial short stature, developmental delay and distinctive facies.
• The most common signs at this state are multiple congenital joint contractures, dysmorphic features with mask-like face, blepharophimosis, ptosis, micrognathia, cleft or high arched palate, low-set ears, arachnodactyly, chest deformation as pectus, kyphoscoliosis and absent deep tendon reflexes are frequent minor malformations have also been described and consist of renal anomalies, cardiovascular abnormalities, hypospadias, omphalomesenteric duct, hypertrophic pyloric stenosis and duodenal bands, hypoplastic right lower lobe of the lung, displacement of the larynx to the right and vertebral abnormalities, cerebral malformations.
• Clinical features found in Njølstad syndrome include: facial and limbs lymphedema, facial abnormalities (thin upper lip, protruding ears), pectus excavatum and vulvar and labial edema.
• In 2001, Martinez-Ferro worked with pectus carinatum patients, providing a nonsurgical treatment of their condition using dynamic compression braces, building on work of Brazilian orthopedist Sydney Haje and coworkers.
• Head white tinged with buff; palpi crimson at base, black at tips; frons at sides and antennae black; thorax brown buff, the patagia with black spots; pectus dark brown in front; crimson streaks below the wings; the fore coxae and femora above crimson, the tibiae and tarsi black above; abdomen crimson, the base, tip of anal tuft and ventral surface buff, a dorsal series of black bands except at base, lateral series of spots and sublateral spots on medial segments.
• The head and thorax are ochreous tinged with fulvous; palpi and sides of frons black; a large black patch on prothorax with streak from it to metathorax; pectus black; femora crimson fringed with ochreous hair, the tibiae and tarsi black; abdomen pale crimson with a blackish dorsal streak on medial segments, the ventral surface ochreous, lateral and sublateral black points on medial segments.
• Legs orange buff ringed with brown; pectus buff; palpi orange buff, extreme tip of third segment brown; head orange buff; antennae pale brown; thorax orange buff with black dots on tegulae and patagia; abdomen buff washed with a darker shade.
• Head and thorax yellowish white; palpi, a patch on frons, tegulae, patagia, and dorsal stripe on thorax black; pectus and stripes on legs black; mid and hind femora orange above; abdomen orange with dorsal black bands, lateral stripes and ventral series of spots.
• Haje (16 February 1952 – 26 June 2012) was a Brazilian orthopedist, known internationally for his pioneering work on chest wall deformities including the creation of a conservative treatment protocol for the pectus carinatum and pectus excavatum conditions.
• A missense mutation in the FAM120AOS protein from amino acid threonine at position 248 to isoleucine (T248I) has been linked in one whole-of-exome sequencing study to: coarse facial features, scoliosis, pectus excavatum, skin laxity, hypotonia, GERD, hyperreactive airway disease, and undescended testicles.
• Guizar-Vasquez-Sanchez-Manzano syndrome is an extremely rare genetic and congenital disorder that is characterized by facial dysmorphisms (more specifically, chubby cheeks, mild frontal bossing, a beaked nose with an accompanying low nasal bridge, malar hypoplasia, peculiar philtrums and upper lips), pectus carinatum, and joint hypermobility.
• Small feet and hands, small shoulders accompanied with short clavicles, clinodactyly, pectus excavatum, mild limb shortening, cardiomegaly, and pulmonic stenosis murmur have also been reported.
• It consists of the following symptoms: disproportionately short stature, shortened upper and lower limbs, generalized shortening and broadening of the fingers alongside small hands, narrow chest, generalized rib anomalies, pectus excavatum, larynx, tracheal, and costal calcifications, frontal bossing, hypertelorism, eye prominence, flat and short nose, wide nostrils, high-arched palate, long philtrum, platyspondyly, and abnormalities of the epiphyses and metaphyses which can be observed on radiographs.
• Other features that may be found in patients with this condition include short stature, dental eruption delay, dental malocclusion, vitiligo, seizures, pectus carinatum, kyphosis, kyphoscoliosis, ventriculomegaly, vasculitis, Raynaud's phenomenon, pain affecting the lower limbs, chronic headaches, chronic kidney disease, cranio-facial dysmorphisms, hypoplasia of the iliac bones, lupus nephritis, arthralgia, arthritis, hypocomplementemia, low to absent TRAP enzyme in serum, high levels of interferon-alpha in the serum, and an over-expression of interferon-stimulated genes.
• Lymphedema-posterior choanal atresia syndrome is a rare genetic disorder characterized by the early-onset appearance of lymphedemas and congenital choanal atresia, which might be accompanied by other features such as pectus excavatum, hypoplasia of the nipples, and facial dysmorphisms such as hypertelorism, frontal bossing, etc.

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