Possible Causes for average intelligence Parkinson Disease Parkinson's disease is a form of neurological disorder characterized by gradual loss of those neurological functions that governs body movement. The disease is therefore also referred to as movement disorder. In the early stages of the disease, signs and symptoms are pretty less evident. However, as the disease[…] [symptoma.com] Rolandic Epilepsy Tiziana Zilli, Sergio Zanini, Stefania Conte, Renato Borgatti and Cosimo Urgesi, Neuropsychological assessment of children with epilepsy and average intelligence using NEPSY [doi.org] RESULT: the obtained data indicate that although intellectual efficiency (measured through the Intelligence Quatient - IQ) was within average, children with rolandic epilepsy [ncbi.nlm.nih.gov] Learning disability: An abnormal condition affecting children of normal or above-average intelligence, characterized by difficulty in learning fundamentals such as reading [childneurologyfoundation.org] Mucopolysaccharidosis Morquio A presents average intelligence, and MPS type VI points to deficits partially related to sensory impairment, implying significant differences between them. [lifescienceglobal.com] Syringomyelia OBJECT: Hindbrain herniation syndrome, or Chiari malformation Type I (CM-I), occurs frequently with craniovertebral junction (CVJ) abnormalities when there is reduction in the posterior fossa volume. Syringomyelia is often present. Posterior fossa dorsal decompression (PFDD) is typically performed but has adverse[…] [ncbi.nlm.nih.gov] Motor Neuron Disease Motor neuron disease (MND) is occasionally aggravated by chronic infection. A misdiagnosed case of tuberculosis with MND is illustrated in a 45-year-old woman who underwent successful VATS wedge excision, which is presented herein. MND in an adult is a rare clinical entity. In order to facilitate the preoperative[…] [ncbi.nlm.nih.gov] Amyotrophic Lateral Sclerosis Please log in to edit this article. Edit Synonyms: ALS, Lou Gehrig’s Disease German : Amyotrophe Lateralsklerose 1 Definition Amyotrophic lateral sclerosis (ALS) is a chronic neurodegenerative disease of the central nervous system (CNS). It affects the motoric system leading to atrophy of skeletal muscles and[…] [flexikon.doccheck.com] Hallermann-Streiff Syndrome The average final height for females is about 60 in (152 cm) and for males it is about 61 in (155 cm). [encyclopedia.com] Most individuals are of normal intelligence; however, it is estimated that 15-30% of individuals with Hallermann-Streiff syndrome show some degree of mental impairment or [encyclopedia.com] Chorea Gravidarum Treatment of a case of severe chorea gravidarum with haloperidol is presented. A possible neuropharmacologic explanation of the beneficial effects of the neuroleptics, particularly haloperidol, is offered based on the dopamine antagonism of these drugs. Heightened dopaminergic activity in the striatum is postulated[…] [ncbi.nlm.nih.gov] Movement Disorder Movement disorder Specialty Neurology Psychiatry Movement disorders are clinical syndromes with either an excess of movement or a paucity of voluntary and involuntary movements, unrelated to weakness or spasticity.[1] Movement disorders are synonymous with basal ganglia or extrapyramidal diseases.[2] Movement[…] [en.wikipedia.org] Spinal Muscular Atrophy The brain is not affected, and they have been tested to have at least average to above average intelligence. [smasupport.com] Some even have above-average intelligence. Encourage your child to take part in as many age-appropriate activities as possible. [healthline.com] When there are no brain abnormalities, the child may have average or above average intelligence, even if there is advanced hydrocephalus at birth. [aans.org] Mucopolysaccharidosis Type 4A On clinical examination, the child appeared to have a less than average intelligence but was placid and cooperative. [ijaweb.org] Adult Spinal Muscular Atrophy The brain is not affected, and they have been tested to have at least average to above average intelligence. [smasupport.com] Pseudoachondroplasia They have normal intelligence and an average life span. Ongoing medical monitoring is important for people with pseudoachondroplasia. [chop.edu] Intelligence is normal. The average height of adults is 118 cm (males: 86-127 cm; females 104-122 cm). [rgauk.org] People with pseudoachondroplasia have normal intelligence, head size, and facial features. [chop.edu] Achondroplasia No, people with achondroplasia have average intelligence and life expectancy. [growingstronger.org] However, the symptoms can be managed to improve the individual’s overall quality of life Most individuals reach an average height of 4-5 feet. [dovemed.com] Intelligence is usually not affected by the mutated FGFR3 gene, and hence, they are able to lead relatively normal lives Preventative measures, appropriate and timely management [dovemed.com] SHORT Syndrome […] to above-average intelligence. [autism-society.org] Although these children may also possess signs of low blood sugar or obesity, they display average body proportions and (average intelligence. [hgfound.org] Intelligence or cognitive abilities are unlikely to be affected unless the person has hydrocephalus, or too much fluid around the brain. [medicalnewstoday.com] Spinal Muscular Atrophy Type 1 The brain is not affected, and they have been tested to have at least average to above average intelligence. [smasupport.com] Some even have above-average intelligence. Encourage your child to take part in as many age-appropriate activities as possible. [healthline.com] Hearing and vision are not affected, and intelligence is normal or above average. [christopherreeve.org] Craniosynostosis From Wikidata Jump to navigation Jump to search synostosis that results in premature fusion located in skull craniostenosis premature closure of cranial sutures craniosynostosis syndrome edit English craniosynostosis synostosis that results in premature fusion located in skull craniostenosis premature closure of[…] [wikidata.org] Craniofrontonasal Dysplasia In conclusion, individuals diagnosed with frontonasal dysplasia usually are of average intelligence and can expect a normal life span. [ruralneuropractice.com] Osteogenesis Imperfecta Type 13 OMIM : 57 Osteogenesis imperfecta (OI) is a connective tissue disorder characterized by bone fragility and low bone mass. Due to considerable phenotypic variability, Sillence et al. (1979) developed a classification of OI subtypes based on clinical features and disease severity: OI type I, with blue sclerae (166200);[…] [malacards.org] Russell-Silver Syndrome The Russell-Silver syndrome's phenotypic features consist of musculoskeletal abnormalities, genitourinary malformations, craniofacial dysmorphy and cutaneous dyschromia, which is usually reported as café au lait spots. We present the first instances of a large, unilateral, achromic patch as an additional cutaneous[…] [ncbi.nlm.nih.gov] Mucopolysaccharidosis Type 6 Summary Epidemiology Birth prevalence is between 1 in 43,261 and 1 in 1,505,160 live births. Clinical description The disorder shows a wide spectrum of symptoms from slowly to rapidly progressing forms. The characteristic skeletal dysplasia includes short stature, dysostosis multiplex and degenerative joint disease.[…] [orpha.net] Mucopolysaccharidosis Type 1S Mucopolysaccharidosis 5 is nowadays referred to as mucopolysaccharidosis 1S or Scheie syndrome. Mucopolysaccharidosis 5 is now classified as a form of mucopolysaccharidosis 1, referred to as mucopolysaccharidosis 1S (MPS1S) or Scheie syndrome. MPS1S is the mildest form of mucopolysaccharidosis 1. [symptoma.com] Nemaline Myopathy Type 5 J Biol Chem. 2005 Apr 8;280(14):13241-9. Epub 2005 Jan 23. Author information 1 Section of Molecular Cardiology, Evanston Northwestern Healthcare and Northwestern University Feinberg School of Medicine, Evanston, Illinois 60201, USA. Abstract A nonsense mutation at codon Glu180 in exon 11 of slow skeletal muscle[…] [ncbi.nlm.nih.gov] Rheumatic Chorea Intellectual impairment has been reported in one family in which affected individuals had intelligence quotient scores averaging 10 points lower than unaffected relatives. [emedicine.medscape.com] Primary Torsion Dystonia Abstract A GAG deletion in the DYT1 gene accounts for most early, limb onset primary torsion dystonia (PTD). The genetic bases for the more common adult onset and focal PTD are less well delineated. Genetic loci for an "intermediate dystonia" phenotype and for torticollis, named DYT6 and DYT7 respectively, have[…] [ncbi.nlm.nih.gov] Fraser Syndrome Fraser syndrome is an uncommon genetic disorder characterized by multiple congenital abnormalities. Newborns afflicted with this syndrome have abnormalities of the eyes, ears, nose, larynx, palate, extremities and urogenital system. A review of the literature shows a deficiency in the description of the ENT[…] [ncbi.nlm.nih.gov] Spondyloepimetaphyseal Dysplasia Type Strudwick The children were judged to be of average intelligence; earlier, mental retardation was thought to be present and to distinguish their disorder from Strudwick dysplasia. [bio2rdf.org] Mulibrey Nanism Syndrome Post by first » Sat Mar 2, 2019 12:20 am Please, help me to find this enanismo de mulibrey pdf file. Thanks! Mulibrey nanism - Wikipedia ; Mulibrey nanism also called Perheentupa syndrome and pericardial constriction with growth failure, is a rare autosomal recessive congenital disorder. It causes severe growth failure[…] [wsvrzbou.tk] SAMS Syndrome A second girl with the unique combination of auditory canal atresia and scapulohumeral synostosis is reported. This patient also had bilateral clubfeet and genital abnormalities. The other patient reported with this syndrome and the presently reported child both had consanguineous parents. Mental development was[…] [ncbi.nlm.nih.gov] Facioauriculoradial Dysplasia MalaCards integrated aliases for Phocomelia-Ectrodactyly, Ear Malformation, Deafness, and Sinus Arrhythmia: Name: Phocomelia-Ectrodactyly, Ear Malformation, Deafness, and Sinus Arrhythmia 57 Phocomelia-Ectrodactyly-Deafness-Sinus Arrhythmia Syndrome 59 Facioauriculoradial Dysplasia 57 Stoll-Lévy-Francfort Syndrome[…] [malacards.org]
