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Congenital scalp defects: Adams-Oliver syndrome. A case report and review of the literature.
Arand AG, Ball WS, Crone KR. Arand AG, et al. Pediatr Neurosurg. 1991-1992;17(4):203-7. doi: 10.1159/000120598. Pediatr Neurosurg. 1991. PMID: 1822137 Review.
First described 160 years ago, ACC is recognized as a heterogenous group of disorders all having focal absence of scalp. Type III ACC, Adams-Oliver syndrome, consists of a scalp defect associated with a distal limb anomaly. ...Larger lesions associated with u …
First described 160 years ago, ACC is recognized as a heterogenous group of disorders all having focal absence of scalp. Type III ACC, Ad
Congenital scalp defects with distal limb anomalies (Adams-Oliver syndrome): report of ten cases and review of the literature.
Küster W, Lenz W, Kääriäinen H, Majewski F. Küster W, et al. Am J Med Genet. 1988 Sep;31(1):99-115. doi: 10.1002/ajmg.1320310112. Am J Med Genet. 1988. PMID: 3066221 Review.
We describe one family with 5 affected persons in 4 generations, another family with 2 affected brothers and 3 sporadic cases of the rare syndrome of congenital scalp defects with distal limb deficiency. ...
We describe one family with 5 affected persons in 4 generations, another family with 2 affected brothers and 3 sporadic cases of the …
Idiopathic non-cirrhotic portal hypertension: a review.
Schouten JN, Verheij J, Seijo S. Schouten JN, et al. Orphanet J Rare Dis. 2015 May 30;10:67. doi: 10.1186/s13023-015-0288-8. Orphanet J Rare Dis. 2015. PMID: 26025214 Free PMC article. Review.
.), 2) chronic infections, 3) exposure to medications or toxins (e.g. azathioprine, 6- thioguanine, arsenic), 4) genetic predisposition (i.e. familial aggregation and association with Adams-Oliver syndrome and Turner disease) and 5) prothrombotic condi …
.), 2) chronic infections, 3) exposure to medications or toxins (e.g. azathioprine, 6- thioguanine, arsenic), 4) genetic predispositi …
Dermatoscopy of Common Lesions in Pediatric Dermatology.
Micali G, Verzì AE, Quattrocchi E, Ng CY, Lacarrubba F. Micali G, et al. Dermatol Clin. 2018 Oct;36(4):463-472. doi: 10.1016/j.det.2018.05.012. Epub 2018 Aug 16. Dermatol Clin. 2018. PMID: 30201155 Review.
Congenital cardiac malformations in Adams-Oliver syndrome.
Zapata HH, Sletten LJ, Pierpont ME. Zapata HH, et al. Clin Genet. 1995 Feb;47(2):80-4. doi: 10.1111/j.1399-0004.1995.tb03928.x. Clin Genet. 1995. PMID: 7606848 Review.
Two patients with Adams-Oliver syndrome and congenital cardiac malformations are described. A literature review revealed at 13.4% occurrence of congenital cardiac malformations in individuals with Adams-Oliver syndrome, suggesting …
Two patients with Adams-Oliver syndrome and congenital cardiac malformations are described. A literature review reveale …
Adams-Oliver syndrome associated with cardiovascular malformations.
Lin AE, Westgate MN, van der Velde ME, Lacro RV, Holmes LB. Lin AE, et al. Clin Dysmorphol. 1998 Oct;7(4):235-41. doi: 10.1097/00019605-199810000-00001. Clin Dysmorphol. 1998. PMID: 9823488 Review.
We describe two families with Adams-Oliver syndrome (AOS), an autosomal dominant malformation syndrome (MIM No. 10030), in which cardiovascular malformations (CVMs) have been reported previously. ...
We describe two families with Adams-Oliver syndrome (AOS), an autosomal dominant malformation syndrome (MIM No. 10030), …
Multiomics Integration in Skin Diseases with Alterations in Notch Signaling Pathway: PlatOMICs Phase 1 Deployment.
Brandão LAC, Tricarico PM, Gratton R, Agrelli A, Zupin L, Abou-Saleh H, Moura R, Crovella S. Brandão LAC, et al. Int J Mol Sci. 2021 Feb 3;22(4):1523. doi: 10.3390/ijms22041523. Int J Mol Sci. 2021. PMID: 33546374 Free PMC article. Review.
We considered the pathologies of five human skin diseases, Hidradenitis Suppurativa, Dowling Degos Disease, Adams-Oliver Syndrome, Psoriasis, and Atopic Dermatitis, in which the molecular alterations in the Notch signaling pathway have been reported. ...
We considered the pathologies of five human skin diseases, Hidradenitis Suppurativa, Dowling Degos Disease, Adams-Oliver Sy
Adams-Oliver syndrome in siblings with central nervous system findings, epilepsy, and developmental delay: refining the features of a severe autosomal recessive variant.
McGoey RR, Lacassie Y. McGoey RR, et al. Am J Med Genet A. 2008 Feb 15;146A(4):488-91. doi: 10.1002/ajmg.a.32163. Am J Med Genet A. 2008. PMID: 18203152 Review.
Adams-Oliver syndrome (AOS) is a well-known rare syndrome of cutis aplasia in combination with limb defects. ...
Adams-Oliver syndrome (AOS) is a well-known rare syndrome of cutis aplasia in combination with limb defects. ...
Aplasia cutis congenita, terminal limb defects and periventricular leukomalacia in one sibling with minor findings in the other-probable autosomal recessive Adams-Oliver Syndrome.
Balasubramanian M, Collins AL. Balasubramanian M, et al. Eur J Med Genet. 2009 Jul-Aug;52(4):234-8. doi: 10.1016/j.ejmg.2009.04.005. Epub 2009 May 4. Eur J Med Genet. 2009. PMID: 19416763 Review.
We report on siblings with probable Adams-Oliver syndrome. The older brother had symmetric intra-uterine growth retardation, plagiocephaly, a cardiac defect and periventricular calcification. ...Prenatal cranial imaging in the younger sibling suggested possib …
We report on siblings with probable Adams-Oliver syndrome. The older brother had symmetric intra-uterine growth retarda …
A case of Adams-Oliver syndrome associated with acrania, microcephaly, hemiplegia, epilepsy, and mental retardation.
Caksen H, Kurtoğlu S. Caksen H, et al. Acta Neurol Belg. 2000 Dec;100(4):252-5. Acta Neurol Belg. 2000. PMID: 11233683 Review.
Adams-Oliver syndrome (AOS) is a rare congenital disorder, characterized by aplasia cutis congenita (ACC) of the scalp and variable degrees of terminal transverse limb defects. ...
Adams-Oliver syndrome (AOS) is a rare congenital disorder, characterized by aplasia cutis congenita (ACC) of the scalp
11 results