salicylic acid has been researched along with Microcephaly in 18 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).
Microcephaly: A congenital abnormality in which the CEREBRUM is underdeveloped, the fontanels close prematurely, and, as a result, the head is small. (Desk Reference for Neuroscience, 2nd ed.)
| 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) |
| "Massive subgaleal hematoma is defined as profuse bleeding in the subgaleal layer of the scalp, causing excessive accumulation of hematoma, thus progressively increasing the size of head circumference." | 1.91 | Massive subgaleal hematoma: a potentially fatal rare entity-a case-based review. ( Faried, A; Halim, D, 2023) |
| "The sister had microcephaly, periventricular calcifications, minor retinal vasculopathy, and mild impaired neurodevelopment, but only very subtle limb abnormalities and no ACC." | 1.72 | Intrafamilial phenotypic variability in autosomal recessive DOCK6-related Adams-Oliver syndrome. ( Aguirre-Guillén, RL; Bobadilla-Morales, L; Corona-Rivera, A; Corona-Rivera, JR; Pacheco-Torres, PA; Peña-Padilla, C; Quezada-Salazar, CA; Rivera-Montellano, ML; Schanze, D; Schanze, I; Zenker, M; Zepeda-Romero, LC, 2022) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 6 (33.33) | 18.7374 |
| 1990's | 6 (33.33) | 18.2507 |
| 2000's | 4 (22.22) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 2 (11.11) | 2.80 |
| Authors | Studies |
|---|---|
| Zepeda-Romero, LC | 1 |
| Zenker, M | 1 |
| Schanze, D | 1 |
| Schanze, I | 1 |
| Peña-Padilla, C | 1 |
| Quezada-Salazar, CA | 1 |
| Pacheco-Torres, PA | 1 |
| Rivera-Montellano, ML | 1 |
| Aguirre-Guillén, RL | 1 |
| Bobadilla-Morales, L | 2 |
| Corona-Rivera, A | 2 |
| Corona-Rivera, JR | 2 |
| Halim, D | 1 |
| Faried, A | 1 |
| KRATTER, FE | 1 |
| Urbani, CE | 1 |
| Russell, LJ | 1 |
| Weaver, DD | 2 |
| Bull, MJ | 2 |
| Weinbaum, M | 1 |
| Alexander, IE | 1 |
| Tauro, GP | 1 |
| Bankier, A | 1 |
| Pascual-Castroviejo, I | 1 |
| Roche, MC | 1 |
| Martinez Fernández, V | 1 |
| Perez-Romero, M | 1 |
| Escudero, RM | 1 |
| Garcia-Peñas, JJ | 1 |
| Sanchez, M | 1 |
| Zoll, B | 1 |
| Wolf, J | 1 |
| Lensing-Hebben, D | 1 |
| Pruggmayer, M | 1 |
| Thorpe, B | 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 |
| Caksen, H | 1 |
| Kurtoğlu, S | 1 |
| Corona-Rivera, E | 1 |
| Romero-Velarde, E | 1 |
| Hernández-Rocha, J | 1 |
| Marble, M | 1 |
| Pridjian, G | 1 |
| Smith, DW | 1 |
| Greely, MJ | 1 |
| Katalin, K | 1 |
| Magdolna, M | 1 |
| Péter, L | 1 |
| Moore, CA | 1 |
| Bönnemann, CG | 1 |
| Meinecke, P | 1 |
| Weninger, M | 1 |
| Simbruner, G | 1 |
| Malamitsi-Puchner, A | 1 |
| Kelch, RP | 1 |
| Janzen, MK | 1 |
| Gall, JC | 1 |
3 reviews available for salicylic acid and Microcephaly
| 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 |
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 |
Report and review of the fetal brain disruption sequence.
Topics: Abnormalities, Multiple; Brain; Diagnosis, Differential; Electroencephalography; Fetal Diseases; Hum | 2001 |
15 other studies available for salicylic acid and Microcephaly
| Article | Year |
|---|---|
Intrafamilial phenotypic variability in autosomal recessive DOCK6-related Adams-Oliver syndrome.
Topics: Biological Variation, Population; Ectodermal Dysplasia; Female; Guanine Nucleotide Exchange Factors; | 2022 |
Massive subgaleal hematoma: a potentially fatal rare entity-a case-based review.
Topics: Child; Female; Hematoma; Hemorrhage; Humans; Microcephaly; Scalp; Skull | 2023 |
Case of cutis verticis gyrata in a low-grade microcephalic spastic male.
Topics: Connective Tissue Diseases; Disease; Humans; Male; Medical Records; Microcephaly; Muscle Spasticity; | 1958 |
Aplasia cutis congenita, polythelia, microcephaly, and developmental delay: a unique expression of polytopic field defect involving possible 'paradominant' inheritance?
Topics: Abnormalities, Multiple; Child; Developmental Disabilities; Ectodermal Dysplasia; Genes, Dominant; H | 2004 |
In utero brain destruction resulting in collapse of the fetal skull, microcephaly, scalp rugae, and neurologic impairment: the fetal brain disruption sequence.
Topics: Adult; Anencephaly; Brain; Cranial Sutures; Female; Gestational Age; Humans; Hydranencephaly; Infant | 1984 |
Fetal brain disruption sequence in sisters.
Topics: Biopsy; Bone Marrow; Brain; Cephalometry; Child, Preschool; Diagnosis, Differential; Female; Follow- | 1995 |
Incontinentia pigmenti: MR demonstration of brain changes.
Topics: Adolescent; Adult; Agenesis of Corpus Callosum; Atrophy; Brain; Cerebellar Ataxia; Cerebellum; Child | 1994 |
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 |
Scalp defects, polythelia, microcephaly, and developmental delay: a new syndrome with apparent autosomal dominant inheritance.
Topics: Abnormalities, Multiple; Adult; Child; Child, Preschool; Developmental Disabilities; Family Health; | 2002 |
Unruly scalp hair in infancy: its nature and relevance to problems of brain morphogenesis.
Topics: Brain; De Lange Syndrome; Down Syndrome; Hair; Humans; Infant; Infant, Newborn; Microcephaly; Morpho | 1978 |
[Indication and value of trichoglyphic examinations].
Topics: Child, Preschool; Female; Gestational Age; Hair; Humans; Intellectual Disability; Male; Microcephaly | 1977 |
Fetal brain disruption sequence.
Topics: Abnormalities, Multiple; Brain; Female; Humans; Infant, Newborn; Male; Microcephaly; Scalp; Skull | 1990 |
Fetal brain disruption sequence: a milder variant.
Topics: Facial Bones; Female; Humans; Infant, Newborn; Microcephaly; Radiography; Scalp; Skull; Tomography | 1990 |
Heat flux from the head surface in healthy newborns and in newborns with cerebral pathology.
Topics: Asphyxia Neonatorum; Heart Defects, Congenital; Humans; Hydrocephalus; Hypoxia, Brain; Infant, Newbo | 1989 |
Multiple congenital anomalies in an infant with an elongated B-group chromosome.
Topics: Abnormalities, Multiple; Chromosome Aberrations; Chromosomes, Human, 4-5; Facial Expression; Facial | 1969 |