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Page "Rett syndrome" ¶ 93
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Congenital and variant
Congenital glomus tumors are rare ; they are plaquelike in appearance and are considered a variant of multiple glomus tumors.

Congenital and severe
" These included, for the Nazis, those suffering from " Congenital Mental Deficiency ", schizophrenia, " Manic-Depressive Insanity ", " Hereditary Epilepsy ", " Hereditary Chorea " ( Huntington ’ s ), Hereditary Blindness, Hereditary Deafness, " any severe hereditary deformity ", as well as " any person suffering from severe alcoholism ".
Congenital insensitivity to pain with anhidrosis may be misdiagnosed for leprosy, based on similar symptoms of severe injuries to the hands and feet.
Congenital generalized hypertrichosis causes males to exhibit excessive facial and upper body hair, whereas women exhibit less severe asymmetrical hair distribution.
Congenital forms of hyperinsulinemic hypoglycemia can be transient or persistent, mild or severe.
The tale is the basis for " Ondine's Curse ," the historical name for Congenital Central Hypoventilation Syndrome ( CCHS ), a severe form of sleep apnea.
* Congenital and acquired causes of muscle weakness may be severe enough to limit breathing and cause hypoxemia, as can muscle weakness and then fatigue in extreme cases of COPD.

Congenital and syndrome
# Congenital: Children of a healthy mother can, very rarely, develop myasthenic symptoms beginning at birth, congenital myasthenic syndrome or CMS.
Congenital genetic disease is well understood, and it is also clear that epigenetics can play a role, for example, in the case of Angelman syndrome and Prader-Willi syndrome.
Congenital heart disease needs to be explored in every female newly diagnosed with Turner syndrome.
* Congenital myasthenic syndrome, An inherited neuromuscular disorder
Other names for the syndrome include Abdominal Muscle Deficiency Syndrome, Congenital Absence of the Abdominal Muscles, Eagle-Barrett Syndrome, Obrinsky Syndrome, Fröhlich Syndrome, or rarely, Triad Syndrome.
Congenital rubella syndrome ( CRS ) can occur in a developing fetus of a pregnant woman who has contracted rubella during her first trimester.
::* Congenital generalized lipodystrophy ( Beradinelli-Seip syndrome )
* Congenital rubella syndrome, a disease passed from mother to fetus
* Congenital rubella syndrome
Congenital problems include Long QT syndrome and Catecholaminergic polymorphic ventricular tachycardia.
Congenital VSDs are frequently associated with other congenital conditions, such as Down syndrome.
Amniotic band syndrome ( also known as " ADAM complex ", " Amniotic band sequence ", " Congenital constriction bands " and " Pseudoainhum ") is a congenital disorder caused by entrapment of fetal parts ( usually a limb or digits ) in fibrous amniotic bands while in utero.
# Congenital myasthenic syndrome
* Congenital asplenia ( rare ) may be due to genetic disorders, ( i. e. heterotaxy syndrome ).
* Congenital rubella syndrome
Other names for this condition include: Duane's Retraction Syndrome ( or DR syndrome ), Eye Retraction Syndrome, Sausage Eye, Retraction Syndrome, Congenital retraction syndrome and Stilling-Turk-Duane Syndrome.
Congenital long-QT syndrome and drugs that prolong the PR or QRS interval are contraindications to dolasetron therapy.

Congenital and development
* Congenital anomaly, popularly referred to as a birth defect, a disorder present at birth, the result of an inherited gene mutation, an error during morphogenesis or fetal development, or an environmental factor
* Congenital diaphragmatic hernia, a disorder involving abnormal development of the diaphragm
Congenital TEF can arise due to failed fusion of the tracheoesophageal ridges during the third week of embryological development.
Congenital and acquired jing have a promoting / controlling relationship with each other and their interaction produces kidney jing ; all three play a part in determining growth and development, sexual maturation, reproduction, and aging.
* Congenital Bilateral Absence of the Vas deferens ( CBAVD ) due to increased mucus thickness during foetal development

Congenital and patients
** Congenital adrenal hyperplasias are genetic defects of enzymes involved in cortisol production and can affect sex characteristics of affected patients.
Several clinical trials have already reported positive results using rAAV to treat Leber's Congenital Amaurosis, showing that the therapy was both safe and effective There were no serious adverse events, and patients in all three studies showed improvement in their visual function as measured by a number of methods.
* Congenital heart disease — especially patent ductus arteriosus ( 50 % of patients )
Myotonia is a symptom commonly seen in patients with myotonic muscular dystrophy, of which two documented types and one speculated type exist, and, in a group of disorders called channelopathies ( hereditary diseases that are caused by mutations in the chloride, sodium or potassium ion transport channels in the muscle membrane ), such as Myotonia Congenita ( Congenital Myotonia ) of which two types called Becker's Disease and Thomsen's Disease exist.
All patients with unrepaired or repaired aortic coarctation require follow up in specialized Congenital Heart Disease centers.
Congenital insensitivity to pain with anhidrosis ( CIPA ), also called hereditary sensory and autonomic neuropathy type IV — is an extremely rare inherited disorder of the nervous system which prevents the sensation of pain, heat, cold, or any real nerve-related sensations ( including feeling the need to urinate ); however, patients can still feel pressure.
· Congenital anomalies occur more frequently in patients with ELS than ILS.

Congenital and their
Congenital lactase deficiency ( CLD ), where the production of lactase is inhibited from birth, can be dangerous in any society because of infants ' nutritional reliance on breast milk during their first months.
Congenital malformations have been reported with the use of ACE inhibitors during the first trimester of pregnancy, while fetal and neonatal toxicity, death, and congenital anomalies have been reported with their use during the second and third trimesters of pregnancy.

Congenital and head
In the play " Almost, Maine " by John Cariani, the vignette " This Hurts " is about a man with Congenital Analgesia, or " Hereditary Sensory Neuropathy Type 4 ", who is clocked in the head with an ironing board, and in the end feels the pain of love.
Congenital diaphragmatic hernia: coronal obstetric ultrasound ( head to right of image, thorax centre, abdomen left ) shows the stomach and heart both within the thorax.

Congenital and are
Congenital heart defects are defects in the structure of the heart which are present at birth.
* Congenital defect – problems or conditions that are present at birth.
Congenital cholesteatomas are usually epidermal cysts which have arisen as a result of a developmental abnormality.
Congenital cholesteatomas are more often found in the anterior aspect of the ear drum, in contrast to acquired cholesteatomas that usually arise from the pars flaccida region of the ear drum in the posterior-superior aspect of the ear drum.
Congenital disorders of glycosylation are sometimes known as CDG syndromes.
Congenital fourth nerve palsies are amenable to surgical treatment.
Disorders referred to as " Congenital Central Hypoventilation Syndrome " or " CCHS " and " Rapid-Onset Obesity, Hypothalamic Dysfunction, Hypoventilation, with Autonomic Dysregulation " or ROHHAD are recognized.
* Congenital dermoids, however, are thought to arise from cells whose position is correct but which fail to differentiate into the correct cell-type.
Congenital adrenal hyperplasias are a family of autosomal recessive diseases resulting from defects in steps of the synthesis of cortisol from cholesterol by the adrenal gland.
All of the issues related to virilization, neonatal assignment, advantages and disadvantages of genital surgery, childhood and adult virilization, gender identity and sexual orientation are similar to those of 21-hydroxylase CAH and elaborated in more detail in Congenital adrenal hyperplasia.
Congenital heart defects are associated with an increased incidence of some other symptoms, together being called the VACTERL association:
Mnemonics are routinely taught to medical students to ensure that all possible pathological processes are considered, for example VINDICATE: Vascular, Inflammatory, Neoplastic, Degenerative / Deficiency, Idiopathic / Intoxication, Congenital, Autoimmune / Allergic, Traumatic, Endocrine
Congenital webs commonly appear in the middle and inferior third of the esophagus, and they are more likely to be circumferential with a central or eccentric orifice.
Congenital forms of hypertrichosis are caused by genetic mutations, and are extremely rare, unlike acquired forms.
Congenital forms of hypertrichosis are rare.
Congenital ear deformities are defined as either malformations ( microtia, cryptotia ) or deformations, wherein the term “ ear deformation ” implies a normal chondrocutaneous component with an abnormal auricular architecture.

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