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Quoted phrase not found in phrase index: "Neu-Laxova syndrome 1"
Page 1
Neu Laxova syndrome.
Dwivedi T, Gosavi M. Dwivedi T, et al. Indian J Pathol Microbiol. 2019 Jan-Mar;62(1):149-152. doi: 10.4103/IJPM.IJPM_351_17. Indian J Pathol Microbiol. 2019. PMID: 30706883
Rare manifestations of Neu-Laxova syndrome.
Badakali M, Badakali A, Dombale V. Badakali M, et al. Fetal Pediatr Pathol. 2012 Feb;31(1):1-5. doi: 10.3109/15513815.2011.618864. Fetal Pediatr Pathol. 2012. PMID: 22233503
Neu-Laxova syndrome is a rare lethal congenital disorder involving multiple systems. ...Therefore, the condition was diagnosed postnatally. Because of the autosomal recessive inheritence of Neu-Laxova syndrome, in countries with high rate …
Neu-Laxova syndrome is a rare lethal congenital disorder involving multiple systems. ...Therefore, the condition was di …
Neu-Laxova syndrome: a case report.
Roy S, Begum J, Sharifunnaher B, Saha AK, Afroza S, Islam MZ. Roy S, et al. Mymensingh Med J. 2014 Jan;23(1):167-9. Mymensingh Med J. 2014. PMID: 24584393
Neu-Laxova syndrome (NLS) is a rare lethal syndrome found in both consanguinous and non-consanguinous couple. ...We are presenting this case in addition from Bangladesh to lend further support to those two new findings as component of Neu-Laxova …
Neu-Laxova syndrome (NLS) is a rare lethal syndrome found in both consanguinous and non-consanguinous couple. ...We are …
Neu-Laxova syndrome: a case report.
Hickey P, Piantanida E, Lentz-Kapua S, Kenner J. Hickey P, et al. Pediatr Dermatol. 2003 Jan-Feb;20(1):25-7. doi: 10.1046/j.1525-1470.2003.03005.x. Pediatr Dermatol. 2003. PMID: 12558841
Neu-Laxova syndrome is a rare congenital disorder characterized by microcephaly, limb contactures, lissencephaly and ichthyosis. A case of Neu-Laxova syndrome is presented, with a discussion of clinical manifestations, complications, and …
Neu-Laxova syndrome is a rare congenital disorder characterized by microcephaly, limb contactures, lissencephaly and ic …
Neu-Laxova syndrome: report of a case and comments.
Karimi-Nejad MH, Khajavi H, Gharavi MJ, Karimi-Nejad R. Karimi-Nejad MH, et al. Am J Med Genet. 1987 Sep;28(1):17-23. doi: 10.1002/ajmg.1320280104. Am J Med Genet. 1987. PMID: 3314507 Review.
We report on an infant with Neu-Laxova syndrome [Neu et al, 1971; Laxova et al, 1972; Povysilova et al, 1976; Lazjuk et al, 1979; Scott et al, 1981; Fitch et al, 1982; Mueller et al, 1983; Turkel et al, 1983; Paes et al, 1985], and emphasize the ichthyotic sk …
We report on an infant with Neu-Laxova syndrome [Neu et al, 1971; Laxova et al, 1972; Povysilova et al, 1976; Lazjuk et …
Cerebro-osseous-digital syndrome: four new cases of a lethal skeletal dysplasia--distinct from Neu-Laxova Syndrome.
Elliott AM, Gonzales M, Hoeffel JC, Le Merrer M, Maroteaux P, Encha-Razavi F, Joye N, Berchel C, Fliegel C, Aughton DJ, Beaudry-Rodgers K, Hasteh F, Nerlich AG, Wilcox WR, Rimoin DL, Lachman RS, Freisinger P. Elliott AM, et al. Am J Med Genet. 2002 Apr 22;109(2):139-48. doi: 10.1002/ajmg.10324. Am J Med Genet. 2002. PMID: 11977163
Neu-Laxova Syndrome (NLS) is a severe disorder with intrauterine growth retardation, edema, and characteristic face (including microcephaly with receding forehead, protuberant eyes, a flattened nose, deformed ears, cleft palate, and micrognathia). ...Scott et …
Neu-Laxova Syndrome (NLS) is a severe disorder with intrauterine growth retardation, edema, and characteristic face (in …
What syndrome is this? Neu-Laxova syndrome.
Carder KR, Fitzpatrick JE, Weston WL. Carder KR, et al. Pediatr Dermatol. 2003 Jan-Feb;20(1):78-80. doi: 10.1046/j.1525-1470.2003.03017.x. Pediatr Dermatol. 2003. PMID: 12558853 No abstract available.
Brief clinical observations: the Neu-Laxova syndrome--a distinct entity.
Lazjuk GI, Lurie IW, Ostrowskaja TI, Cherstvoy ED, Kirillova IA, Nedzved MK, Usoev SS. Lazjuk GI, et al. Am J Med Genet. 1979;3(3):261-7. doi: 10.1002/ajmg.1320030304. Am J Med Genet. 1979. PMID: 225952
We report a stillborn girl with a complex syndrome of microcephaly, lissencephaly, severe subcutaneous edema, atrophic muscles, camptodactyly, syndactyly of toes and fingers, hypoplastic genitalia, and numerous structural changes of the brain and eyes. Similar cases have been rep …
We report a stillborn girl with a complex syndrome of microcephaly, lissencephaly, severe subcutaneous edema, atrophic muscles, camptodactyl …
Second trimester diagnosis of Neu Laxova syndrome.
Shivarajan MA, Suresh S, Jagadeesh S, Lata S, Bhat L. Shivarajan MA, et al. Prenat Diagn. 2003 Jan;23(1):21-4. doi: 10.1002/pd.485. Prenat Diagn. 2003. PMID: 12533807
This is the first report of a prenatally diagnosed case of Neu Laxova syndrome (NLS) from India. This also includes a case of NLS in monochorionic diamniotic twins and two more cases in which we were able to detect most of the features of NLS as early as 19 t …
This is the first report of a prenatally diagnosed case of Neu Laxova syndrome (NLS) from India. This also includes a c …
Sonographic diagnosis of Neu-Laxova syndrome.
Gülmezoĝlu AM, Ekici E. Gülmezoĝlu AM, et al. J Clin Ultrasound. 1994 Jan;22(1):48-51. doi: 10.1002/jcu.1870220110. J Clin Ultrasound. 1994. PMID: 8294578 No abstract available.
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