243 related articles for article (PubMed ID: 8775415)
1. A nine-month-old boy with microcephaly, cataracts, intracerebral calcifications and dysmorphic signs: an additional observation of an autosomal recessive congenital infection-like syndrome?
Wieczorek D; Gillessen-Kaesbach G; Passarge E
Genet Couns; 1995; 6(4):297-302. PubMed ID: 8775415
[TBL] [Abstract][Full Text] [Related]
2. Congenital intrauterine infection like syndrome of microcephaly, intracranial calcification and CNS disease.
Mishra D; Gupta VK; Nandan D; Behal D
Indian Pediatr; 2002 Sep; 39(9):866-9. PubMed ID: 12368535
[No Abstract] [Full Text] [Related]
3. Complex consanguinity associated with short rib-polydactyly syndrome III and congenital infection-like syndrome: a diagnostic problem in dysmorphic syndromes.
al-Gazali LI; Sztriha L; Dawodu A; Varady E; Bakir M; Khdir A; Johansen J
J Med Genet; 1999 Jun; 36(6):461-6. PubMed ID: 10874634
[TBL] [Abstract][Full Text] [Related]
4. Autosomal recessive congenital intrauterine infection-like syndrome of microcephaly, intracranial calcification, and CNS disease.
Reardon W; Hockey A; Silberstein P; Kendall B; Farag TI; Swash M; Stevenson R; Baraitser M
Am J Med Genet; 1994 Aug; 52(1):58-65. PubMed ID: 7977464
[TBL] [Abstract][Full Text] [Related]
5. Syndrome of microcephaly, microphthalmia, cataracts, and intracranial calcification.
Slee J; Lam G; Walpole I
Am J Med Genet; 1999 Jun; 84(4):330-3. PubMed ID: 10340646
[TBL] [Abstract][Full Text] [Related]
6. The autosomal recessive congenital intrauterine infection-like syndrome of microcephaly, intracranial calcification, and CNS disease: report of another Bedouin family.
al-Dabbous R; Sabry MA; Farah S; al-Awadi SA; Simeonov S; Farag TI
Clin Dysmorphol; 1998 Apr; 7(2):127-30. PubMed ID: 9571284
[TBL] [Abstract][Full Text] [Related]
7. Cerebro-oculo-facio-skeletal (COFS) syndrome. The variability of presenting symptoms as a manifestation of two subtypes?
Casteels I; Wijnants A; Casaer P; Eggermont E; Misotten L; Fryns JP
Genet Couns; 1991; 2(1):43-6. PubMed ID: 1741976
[TBL] [Abstract][Full Text] [Related]
8. Dominant inheritance of microcephaly, short stature and congenital dislocation of the hips.
Newbury-Ecob RA; Young ID
Clin Dysmorphol; 1993 Jan; 2(1):34-8. PubMed ID: 8298736
[TBL] [Abstract][Full Text] [Related]
9. [Genetic syndromes that mimic congenital infections: report of 2 cases].
Thibault M; Leydet J; Tournier-Lasserve E; Crow YJ; Rivier F; Echenne B; Langlois C; Daudet H; Sarda P; Roubertie A
Arch Pediatr; 2011 Dec; 18(12):1297-1301. PubMed ID: 21963371
[TBL] [Abstract][Full Text] [Related]
10. Congenital dysplastic microcephaly and hypoplasia of the brainstem and cerebellum with diffuse intracranial calcification.
Nakamura K; Kato M; Sasaki A; Kanai M; Hayasaka K
J Child Neurol; 2012 Feb; 27(2):218-21. PubMed ID: 21940696
[TBL] [Abstract][Full Text] [Related]
11. Microcephaly, micrognathia, and bird-headed dwarfism: prenatal diagnosis of a Seckel-like syndrome.
Majoor-Krakauer DF; Wladimiroff JW; Stewart PA; van de Harten JJ; Niermeijer MF
Am J Med Genet; 1987 May; 27(1):183-8. PubMed ID: 3300331
[TBL] [Abstract][Full Text] [Related]
12. [Ophthalmological findings in microcephaly-lymphoedema-chorioretinal dysplasia syndrome].
Hatt Brupbacher SC; Job O; Senn P; Dedes W
Klin Monbl Augenheilkd; 2009 Apr; 226(4):344-6. PubMed ID: 19384796
[TBL] [Abstract][Full Text] [Related]
13. A new case of Martsolf syndrome.
Bora E; Cankaya T; Alpman A; Karaca E; Cogulu O; Tekgul H; Ozkinay F
Genet Couns; 2007; 18(1):71-5. PubMed ID: 17515302
[TBL] [Abstract][Full Text] [Related]
14. New syndromes of mental retardation.
Thurmon TF; Santos CL
Birth Defects Orig Artic Ser; 1975; 11(2):264-8. PubMed ID: 1227531
[TBL] [Abstract][Full Text] [Related]
15. [Acceleration of bone maturation and dysmorphic syndrome in 2 siblings (Marshall-Weaver syndrome)].
Jalaguier J; Montoya F; Germain M; Bonnet H
J Genet Hum; 1983 Dec; 31 Suppl 5():385-95. PubMed ID: 6674414
[TBL] [Abstract][Full Text] [Related]
16. Filippi syndrome: report of three additional cases.
Williams MS; Williams JL; Wargowski DS; Pauli RM; Pletcher BA
Am J Med Genet; 1999 Nov; 87(2):128-33. PubMed ID: 10533026
[TBL] [Abstract][Full Text] [Related]
17. [Trichothiodystrophy: progresssive manifestations].
Foulc P; Jumbou O; David A; Sarasin A; Stalder JF
Ann Dermatol Venereol; 1999 Oct; 126(10):703-7. PubMed ID: 10604009
[TBL] [Abstract][Full Text] [Related]
18. Aicardi-Goutières syndrome: differential diagnosis and aetiopathogenesis.
Lanzi G; D'Arrigo S; Drumbl G; Uggetti C; Fazzi E
Funct Neurol; 2003; 18(2):71-5. PubMed ID: 12911136
[TBL] [Abstract][Full Text] [Related]
19. Galloway-Mowat syndrome of abnormal gyral patterns and glomerulopathy.
Cooperstone BG; Friedman A; Kaplan BS
Am J Med Genet; 1993 Aug; 47(2):250-4. PubMed ID: 8213914
[TBL] [Abstract][Full Text] [Related]
20. Progeroid syndrome with facial teleangiectatic erythema, posterior subcapsular cataracts, calcification of basal ganglia and atrium septum defect type 2.
Fryns JP; Dumoulin M; Hens G
Genet Couns; 1999; 10(4):395-8. PubMed ID: 10631929
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]