142 related articles for article (PubMed ID: 17230486)
1. Severe hypertelorism, midface prominence, prominent/simple ears, severe myopia, borderline intelligence, and bone fragility in two brothers: new syndrome?
Hamamy HA; Teebi AS; Oudjhane K; Shegem NN; Ajlouni KM
Am J Med Genet A; 2007 Feb; 143A(3):229-34. PubMed ID: 17230486
[TBL] [Abstract][Full Text] [Related]
2. Sphenoid sinus agenesis and sella turcica hypoplasia: very rare cases of two brothers with Hamamy syndrome.
Duman SB; Dedeoglu N; Arikan B; Altun O
Surg Radiol Anat; 2020 Nov; 42(11):1377-1380. PubMed ID: 32860086
[TBL] [Abstract][Full Text] [Related]
3. Autosomal recessive inheritance of a syndrome of hypertelorism, hypospadias, and tetralogy of Fallot?
Farag TI; Teebi AS
Am J Med Genet; 1990 Apr; 35(4):516-8. PubMed ID: 2333881
[TBL] [Abstract][Full Text] [Related]
4. Autosomal recessive Robinow syndrome.
Teebi AS
Am J Med Genet; 1990 Jan; 35(1):64-8. PubMed ID: 2301471
[TBL] [Abstract][Full Text] [Related]
5. Ptosis, down-slanting palpebral fissures, hypertelorism, seizures and mental retardation: a possible new MCA/MR syndrome.
Mégarbané A; Le Merrer M; el Kallab K
Clin Dysmorphol; 1997 Jul; 6(3):239-44. PubMed ID: 9220194
[TBL] [Abstract][Full Text] [Related]
6. Dental findings in Hamamy syndrome.
Guler C; Keskin G
Genet Couns; 2014; 25(4):383-7. PubMed ID: 25804015
[TBL] [Abstract][Full Text] [Related]
7. A new autosomal recessive syndrome characterized by ocular hypertelorism, distinctive face, mental retardation, brachydactyly, and genital abnormalities.
Spiegel R; Horovitz Y; Peters H; Erdogan F; Chervinsky I; Shalev SA
Am J Med Genet A; 2009 Dec; 149A(12):2655-60. PubMed ID: 19938075
[TBL] [Abstract][Full Text] [Related]
8. Functional disomy of proximal Xp causes a distinct phenotype comprising early hypotonia, hypertelorism, small hands and feet, ear abnormalities, myopia and cognitive impairment.
Hunter M; Bruno D; Amor DJ
Am J Med Genet A; 2009 Aug; 149A(8):1763-7. PubMed ID: 19610086
[TBL] [Abstract][Full Text] [Related]
9. Anaesthesia and orphan disease: Anaesthetic management of a child with Hamamy syndrome.
Buget MI; Canbolat N; Akgul T; Kucukay S
Eur J Anaesthesiol; 2015 Dec; 32(12):891-3. PubMed ID: 25886715
[No Abstract] [Full Text] [Related]
10. Variable expressivity of hypertelorism in three siblings with Greig syndrome.
Gencik A; Genciková A
Acta Paediatr Hung; 1986; 27(2):133-40. PubMed ID: 3756012
[TBL] [Abstract][Full Text] [Related]
11. Intellectual disability, muscle weakness and characteristic face in three siblings: A newly described recessive syndrome mapping to 3p24.3-p25.3.
Kariminejad A; Nafissi S; Nilipoor Y; Tavasoli A; Van Veldhoven PP; Bonnard C; Ng YT; Majoie CB; Reversade B; Hennekam RC
Am J Med Genet A; 2015 Nov; 167A(11):2508-15. PubMed ID: 26192890
[TBL] [Abstract][Full Text] [Related]
12. New oral findings in Hamamy syndrome.
Banna SA; Hassona Y
Spec Care Dentist; 2018 Nov; 38(6):445-446. PubMed ID: 30171819
[No Abstract] [Full Text] [Related]
13. A new syndrome: multiple congenital abnormalities and mental retardation in two brothers.
Dundar M; Ozdemir SY; Fryns JP
Genet Couns; 2012; 23(1):13-8. PubMed ID: 22611637
[TBL] [Abstract][Full Text] [Related]
14. Hypertelorism, ptosis, and myopia associated with drug-resistant epilepsy, mental delay, growth deficiency, ectodermal defects, and osteopenia.
Zannolli R; Buoni S; Macucci F; Miracco C; de Santi MM; Piomboni P; Bruni E; Malandrini A; Galluzzi P; Hadjistilianou T; Medaglini S; Mazzei MA; Sacco P; Terrosi-Vagnoli P; Volterrani L; Molinelli M; Burlina AB; Swift JA; Fimiani M
Am J Med Genet A; 2004 Jun; 127A(2):212-6. PubMed ID: 15108215
[TBL] [Abstract][Full Text] [Related]
15. Prenatal diagnosis of Opitz (BBB) syndrome in the second trimester by ultrasound detection of hypospadias and hypertelorism.
Hogdall C; Siegel-Bartelt J; Toi A; Ritchie S
Prenat Diagn; 1989 Nov; 9(11):783-93. PubMed ID: 2694153
[TBL] [Abstract][Full Text] [Related]
16. Aphonia, microstomia, deafness, retinal dystrophy, duplicated halluces and intellectual disability.
Kariminejad A; Hennekam RC
Am J Med Genet A; 2012 Nov; 158A(11):2756-62. PubMed ID: 22991300
[TBL] [Abstract][Full Text] [Related]
17. Autosomal recessive tetralogy of Fallot, unusual facies, communicating hydrocephalus, and delayed language development: a new syndrome?
Lammer EJ; Scholes T; Abrams L
Clin Dysmorphol; 2001 Jan; 10(1):9-13. PubMed ID: 11152158
[TBL] [Abstract][Full Text] [Related]
18. Two brothers with Burn-McKeown syndrome.
Wieczorek D; Teber OA; Lohmann D; Gillessen-Kaesbach G
Clin Dysmorphol; 2003 Jul; 12(3):171-4. PubMed ID: 14564154
[TBL] [Abstract][Full Text] [Related]
19. Kabuki make-up syndrome: a syndrome of mental retardation, unusual facies, large and protruding ears, and postnatal growth deficiency.
Niikawa N; Matsuura N; Fukushima Y; Ohsawa T; Kajii T
J Pediatr; 1981 Oct; 99(4):565-9. PubMed ID: 7277096
[TBL] [Abstract][Full Text] [Related]
20. Esophageal atresia, hypoplasia of zygomatic complex, microcephaly, cup-shaped ears, congenital heart defect, and mental retardation--new MCA/MR syndrome in two affected sibs and a mildly affected mother?
Wieczorek D; Shaw-Smith C; Kohlhase J; Schmitt W; Buiting K; Coffey A; Howard E; Hehr U; Gillessen-Kaesbach G
Am J Med Genet A; 2007 Jun; 143A(11):1135-42. PubMed ID: 17497718
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]