salicylic acid has been researched along with Intellectual Disability in 44 studies
Scalp: The outer covering of the calvaria. It is composed of several layers: SKIN; subcutaneous connective tissue; the occipitofrontal muscle which includes the tendinous galea aponeurotica; loose connective tissue; and the pericranium (the PERIOSTEUM of the SKULL).
Intellectual Disability: Subnormal intellectual functioning which originates during the developmental period. This has multiple potential etiologies, including genetic defects and perinatal insults. Intelligence quotient (IQ) scores are commonly used to determine whether an individual has an intellectual disability. IQ scores between 70 and 79 are in the borderline range. Scores below 67 are in the disabled range. (from Joynt, Clinical Neurology, 1992, Ch55, p28)
| Excerpt | Relevance | Reference |
|---|---|---|
| "Now, he is 3 years old, and has microcephaly, moderate mental retardation, left spastic hemiplegia, and epilepsy." | 2.41 | A case of Adams-Oliver syndrome associated with acrania, microcephaly, hemiplegia, epilepsy, and mental retardation. ( Caksen, H; Kurtoğlu, S, 2000) |
| "Congenital melanocytic nevi (CMN) are nevi that are present at birth or arise within the first few weeks of life." | 1.46 | Congenital melanocytic nevus mimicking a turban tumour in an 18-year-old Filipino male. ( Cubillan, E; Sison, MEG; Tansipek, BU, 2017) |
| "Carpenter's syndrome is a relatively rare craniofacial deformity which will occasionally present to craniofacial surgeons for treatment." | 1.29 | Surgical caution with Carpenter's syndrome. ( Poole, MD, 1993) |
| "An electronystagmogram demonstrated periodic alternating nystagmus." | 1.27 | An association of subtotal cerebellar agenesis with organoid nevus--a possible new variety of neurocutaneous syndrome. ( Fukuyama, Y; Hara, M; Izumi, T; Kobayashi, N; Maeda, Y; Wang, PJ; Yajima, K, 1983) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 23 (52.27) | 18.7374 |
| 1990's | 8 (18.18) | 18.2507 |
| 2000's | 8 (18.18) | 29.6817 |
| 2010's | 3 (6.82) | 24.3611 |
| 2020's | 2 (4.55) | 2.80 |
| Authors | Studies |
|---|---|
| Ross, JB | 1 |
| Allderdice, PW | 1 |
| Shapiro, LJ | 1 |
| Aveling, J | 1 |
| Eales, BA | 1 |
| Simms, D | 1 |
| Fozia, F | 1 |
| Shah, K | 1 |
| Nazli, R | 1 |
| Khan, SA | 1 |
| Ahmad, I | 1 |
| Mohammad, N | 1 |
| Khan, S | 1 |
| Alotaibi, A | 1 |
| Sathishkumar, D | 1 |
| Ogboli, M | 1 |
| Moss, C | 1 |
| Sison, MEG | 1 |
| Cubillan, E | 1 |
| Tansipek, BU | 1 |
| Huang, X | 2 |
| Yuan, Q | 1 |
| Luo, Q | 1 |
| Zeng, H | 1 |
| Zheng, X | 1 |
| Yu, Y | 1 |
| Wu, Y | 1 |
| Curatolo, P | 2 |
| Lo-Castro, A | 1 |
| Pinci, M | 1 |
| Moavero, R | 1 |
| Bombardieri, R | 1 |
| Hartman, EC | 1 |
| Gilles, E | 1 |
| McComas, JJ | 1 |
| Danov, SE | 1 |
| Symons, FJ | 1 |
| Blyth, M | 1 |
| Baralle, D | 1 |
| KRATTER, FE | 1 |
| BERG, JM | 1 |
| WINDRATH-SCOTT, A | 1 |
| AKESSON, HO | 3 |
| Schöttler, L | 1 |
| Denisjuk, N | 1 |
| Körber, A | 1 |
| Grabbe, S | 1 |
| Dissemond, J | 1 |
| Wang, PJ | 1 |
| Maeda, Y | 1 |
| Izumi, T | 1 |
| Yajima, K | 1 |
| Hara, M | 1 |
| Kobayashi, N | 1 |
| Fukuyama, Y | 1 |
| Guidetti, V | 1 |
| Garcovich, A | 1 |
| Paolella, A | 1 |
| Bamforth, JS | 1 |
| Kaurah, P | 1 |
| Byrne, J | 1 |
| Ferreira, P | 1 |
| Zoll, B | 1 |
| Wolf, J | 1 |
| Lensing-Hebben, D | 1 |
| Pruggmayer, M | 1 |
| Thorpe, B | 1 |
| Poole, MD | 1 |
| Striano, S | 1 |
| Ruosi, P | 1 |
| Guzzetta, V | 1 |
| Perone, L | 1 |
| Manto, A | 1 |
| Cirillo, S | 1 |
| Chang, GY | 1 |
| Farah, S | 1 |
| Farag, T | 1 |
| Sabry, MA | 1 |
| Simeonov, ST | 1 |
| al-Khattam, S | 1 |
| Abulhassan, SJ | 1 |
| Quasrawi, B | 1 |
| al-Busairi, W | 1 |
| al-Awadi, SA | 1 |
| Koivisto, PA | 1 |
| Koivisto, H | 1 |
| Haapala, K | 1 |
| Simola, KO | 1 |
| Koizumi, T | 1 |
| Caksen, H | 1 |
| Kurtoğlu, S | 1 |
| Fryns, JP | 2 |
| de Cock, P | 1 |
| Filosto, M | 1 |
| Tonin, P | 1 |
| Vattemi, G | 1 |
| Bongiovanni, LG | 1 |
| Rizzuto, N | 1 |
| Tomelleri, G | 1 |
| Keller, K | 1 |
| Williams, C | 1 |
| Seagle, B | 1 |
| Campbell, WW | 1 |
| Buda, FB | 1 |
| Sorensen, G | 1 |
| Katalin, K | 1 |
| Magdolna, M | 1 |
| Péter, L | 1 |
| Mohanty, S | 1 |
| Rao, CJ | 1 |
| Iivanainen, M | 3 |
| Arho, P | 1 |
| Schepis, C | 1 |
| Palazzo, R | 1 |
| Cannavo, SP | 1 |
| Ragusa, RM | 1 |
| Barletta, C | 1 |
| Spina, E | 1 |
| Diven, DG | 1 |
| Solomon, AR | 1 |
| McNeely, MC | 1 |
| Font, RL | 1 |
| Felding, I | 1 |
| Feingold, M | 1 |
| Uyama, E | 1 |
| Teramoto, H | 1 |
| Hashimoto, Y | 1 |
| Okamoto, H | 1 |
| Araki, S | 1 |
| Buttiëns, M | 1 |
| Jonckheere, P | 1 |
| Brouckmans-Buttiëns, K | 1 |
| Van den Berghe, H | 1 |
| Berger, H | 1 |
| Tsuang, MT | 1 |
| Lin, SN | 1 |
| Silvers, DN | 1 |
| Cox, RP | 1 |
| Balis, ME | 1 |
| Dancis, J | 1 |
| Kostiainen, E | 1 |
| Bianchine, JW | 1 |
| Muller, SA | 1 |
| Winkelmann, RK | 1 |
| Palo, J | 1 |
3 reviews available for salicylic acid and Intellectual Disability
| Article | Year |
|---|---|
Trisomy 13 (Patau syndrome) with an 11-year survival.
Topics: Abnormalities, Multiple; Adult; Brain; Child; Child, Preschool; Chromosomes, Human, Pair 13; Female; | 1993 |
[Johanson-Blizzard syndrome].
Topics: Abnormalities, Multiple; Diagnosis, Differential; Exocrine Pancreatic Insufficiency; Growth Disorder | 2000 |
A case of Adams-Oliver syndrome associated with acrania, microcephaly, hemiplegia, epilepsy, and mental retardation.
Topics: Abnormalities, Multiple; Consanguinity; Ectodermal Dysplasia; Epilepsy, Tonic-Clonic; Fingers; Growt | 2000 |
1 trial available for salicylic acid and Intellectual Disability
| Article | Year |
|---|---|
[Clinical efficacy on mental retardation in the children treated with JIN's three scalp needling therapy and the training for cognitive and perceptual disturbance].
Topics: Acupuncture Therapy; Child; Child, Preschool; Cognition; Female; Humans; Intellectual Disability; In | 2015 |
40 other studies available for salicylic acid and Intellectual Disability
| Article | Year |
|---|---|
Familial X-linked ichthyosis, steroid sulfatase deficiency, mental retardation, and nullisomy for Xp223-pter.
Topics: Adult; Child; Chromosome Aberrations; Chromosome Deletion; Female; Gels; Genetic Linkage; Humans; Ic | 1985 |
Novel splicing-site mutation in DCAF17 gene causing Woodhouse-Sakati syndrome in a large consanguineous family.
Topics: Adolescent; Alopecia; Arrhythmias, Cardiac; Basal Ganglia Diseases; Child; Consanguinity; Diabetes M | 2022 |
Classification of aplasia cutis congenita: a 25-year review of cases presenting to a tertiary paediatric dermatology department.
Topics: Abnormalities, Multiple; Child; Child, Preschool; Cleft Palate; Dermatology; Ectodermal Dysplasia; E | 2020 |
Congenital melanocytic nevus mimicking a turban tumour in an 18-year-old Filipino male.
Topics: Adolescent; Diagnosis, Differential; Head and Neck Neoplasms; Humans; Intellectual Disability; Male; | 2017 |
Neuroimaging findings of Sturge-Weber Syndrome in a child with Tuberous Sclerosis.
Topics: Adolescent; Brain; Comorbidity; Epilepsy; Female; Heart Defects, Congenital; Humans; Intellectual Di | 2009 |
Clinical observation of self-injurious behavior correlated with changes in scalp morphology in a child with congenital hydrocephalus.
Topics: Cerebrospinal Fluid Shunts; Child; Craniofacial Abnormalities; Craniotomy; Female; Humans; Hydroceph | 2008 |
Anophthalmia in fronto-facial-nasal dysplasia.
Topics: Abnormalities, Multiple; Adolescent; Anophthalmos; Autistic Disorder; Cleft Lip; Cleft Palate; Crani | 2011 |
The incidence of cutis verticis gyrata in three low-grade mental defectives.
Topics: Connective Tissue Diseases; Disease; Humans; Incidence; Intellectual Disability; Medical Records; Sc | 1958 |
Cutis verticis gyrata with particular reference to its association with mental subnormality.
Topics: Connective Tissue Diseases; Humans; Intellectual Disability; Mental Disorders; Scalp; Skin Diseases | 1962 |
CUTIS VERTICIS GYRATA AND MENTAL DEFICIENCY IN SWEDEN. I. EPIDEMIOLOGIC AND CLINICAL ASPECTS.
Topics: 17-Ketosteroids; Acromegaly; Adrenal Cortex Hormones; Castration; Cerebral Palsy; Chromatography; Co | 1964 |
CUTIS VERTICIS GYRATA AND MENTAL DEFICIENCY IN SWEDEN. II. GENETIC ASPECTS.
Topics: Congenital Abnormalities; Connective Tissue Diseases; Genetics, Medical; Humans; Intellectual Disabi | 1965 |
CUTIS VERTICIS GYRATA THYROAPLASIA AND MENTAL DEFICIENCY.
Topics: Connective Tissue Diseases; Genes; Genetics, Medical; Humans; Intellectual Disability; Pathology; Sc | 1965 |
[Asymptomatic cerebriform folds of the scalp. Diagnosis: primary Cutis verticis gyrata (CVG)].
Topics: Adult; Asphyxia Neonatorum; Biopsy; Chromosome Aberrations; Chromosomes, Human, X; Diagnosis, Differ | 2007 |
An association of subtotal cerebellar agenesis with organoid nevus--a possible new variety of neurocutaneous syndrome.
Topics: Adolescent; Cerebellum; Electronystagmography; Female; Humans; Intellectual Disability; Nevus; Nysta | 1983 |
[Epidermal nervus syndrome].
Topics: Cerebral Palsy; Facial Neoplasms; Facial Paralysis; Female; Humans; Infant; Intellectual Disability; | 1982 |
Adams Oliver syndrome: a family with extreme variability in clinical expression.
Topics: Abnormalities, Multiple; Adult; Brain; Bronchi; Epilepsy; Female; Heart Defects, Congenital; Humans; | 1994 |
Surgical caution with Carpenter's syndrome.
Topics: Acrocephalosyndactylia; Blood Loss, Surgical; Child, Preschool; Cranial Sinuses; Frontal Bone; Human | 1993 |
Cutis verticis gyrata--mental deficiency syndrome: a patient with drug-resistant epilepsy and polymicrogyria.
Topics: Adult; Chromosomes, Human, Pair 16; Chromosomes, Human, Pair 3; Epilepsy; Humans; Intellectual Disab | 1996 |
Cutis verticis gyrata, underrecognized neurocutaneous syndrome.
Topics: Adult; Epilepsy; Humans; Intellectual Disability; Magnetic Resonance Imaging; Male; Scalp; Syndrome | 1996 |
Cutis verticis gyrata-mental deficiency syndrome: report of a case with unusual neuroradiological findings.
Topics: Adult; Brain; Chromosome Inversion; Epilepsy; Humans; Intellectual Disability; Magnetic Resonance Im | 1998 |
A de novo deletion of chromosome 15(q15.2q21.2) in a dysmorphic, mentally retarded child with congenital scalp defect.
Topics: Chromosome Banding; Chromosome Deletion; Chromosomes, Human, Pair 15; Facies; Humans; Infant, Newbor | 1999 |
MCA/MR syndrome with occipital scalp defect and valvular pulmonary stenosis: a cryptic 7pter duplication/18qter deficiency.
Topics: Child; Child, Preschool; Chromosomes, Human, Pair 18; Chromosomes, Human, Pair 7; Humans; Intellectu | 2001 |
Cutis verticis gyrata, mental retardation and Lennox-Gastaut syndrome: a case report.
Topics: Adult; Electroencephalography; Epilepsy, Absence; Humans; Intellectual Disability; Magnetic Resonanc | 2001 |
Klinefelter syndrome and cutis verticis gyrata.
Topics: Acromegaly; Adult; Diagnosis, Differential; Follow-Up Studies; Humans; Intellectual Disability; Kary | 2001 |
Linear nevus sebaceous syndrome: neurological aspects documented by brain scans correlated with developmental history and radiographic studies.
Topics: Brain Diseases; Child; Female; Humans; Intellectual Disability; Nevus; Scalp; Sebaceous Gland Neopla | 1978 |
[Indication and value of trichoglyphic examinations].
Topics: Child, Preschool; Female; Gestational Age; Hair; Humans; Intellectual Disability; Male; Microcephaly | 1977 |
A large cirsoid aneurysm of the scalp associated with epilepsy.
Topics: Aneurysm; Epilepsy; Female; Humans; Infant; Intellectual Disability; Scalp | 1976 |
Skin thickness in cutis verticis gyrata and mental retardation syndrome.
Topics: Adult; Female; Humans; Hypertrophy; Intellectual Disability; Male; Scalp; Skin Diseases; Skinfold Th | 1976 |
Prevalence of primary cutis verticis gyrata in a psychiatric population: association with chromosomal fragile sites.
Topics: Adult; Aged; Aged, 80 and over; Chromosome Fragile Sites; Chromosome Fragility; Female; Fragile X Sy | 1990 |
Nevus sebaceus associated with major ophthalmologic abnormalities.
Topics: Adolescent; Choristoma; Choroid; Coloboma; Eye Abnormalities; Female; Humans; Intellectual Disabilit | 1987 |
Picture of the month. Cutis verticis gyrata.
Topics: Abnormalities, Multiple; Brain; Humans; Infant; Infant, Newborn; Intellectual Disability; Male; Scal | 1988 |
[Two siblings of familial spastic paraplegia with cutis verticis gyrata and mental retardation].
Topics: Adult; Humans; Intellectual Disability; Male; Muscle Spasticity; Paraplegia; Scalp | 1988 |
Scalp defect associated with postaxial polydactyly: confirmation of a distinct entity with autosomal dominant inheritance.
Topics: Adolescent; Fingers; Genes, Dominant; Humans; Intellectual Disability; Male; Radiography; Scalp; Sku | 1985 |
On the electroencephalogram of man. Third report.
Topics: Adolescent; Adult; Anesthesia; Brain Injuries; Cerebral Cortex; Cerebral Hemorrhage; Cerebrovascular | 1969 |
Cutis verticis gyrata in a Chinese mental defective.
Topics: Adult; Cerebral Palsy; Congenital Abnormalities; Electroencephalography; Epilepsy, Tonic-Clonic; Hum | 1974 |
Detection of the heterozygote in Lesch-Nyhan disease by hair-root analysis.
Topics: Adenosine Monophosphate; Athetosis; Clinical Enzyme Tests; Culture Techniques; Female; Fibroblasts; | 1972 |
The electrophoretic pattern of cerebrospinal fluid proteins in the cutis verticis gyrata and mental retardation syndrome.
Topics: Adolescent; Adult; Albumins; Blood Protein Electrophoresis; Cerebral Palsy; Cerebral Ventricles; Cer | 1974 |
The nevus sebaceous of Jadassohn. A neurocutaneous syndrome and a potentially premalignant lesion.
Topics: Adolescent; Adult; Child; Diagnosis, Differential; Ectodermal Dysplasia; Epilepsy; Eye Abnormalities | 1970 |
Trichotillomania. A clinicopathologic study of 24 cases.
Topics: Adolescent; Adult; Alopecia; Biopsy; Child; Child, Preschool; Eyebrows; Eyelashes; Female; Hair; Hum | 1972 |
The cutis verticis gyrata and mental retardation syndrome in a 4-year-old boy.
Topics: Abnormalities, Multiple; Child, Preschool; Humans; Intellectual Disability; Male; Osteoarthropathy, | 1971 |