107 related articles for article (PubMed ID: 25844790)
1. A case of Morfan syndrome.
Hiscox B; Hu J; Young LC
Cutis; 2015 Mar; 95(3):E20-1. PubMed ID: 25844790
[No Abstract] [Full Text] [Related]
2. MORFAN Syndrome: An Infantile Hypoinsulinemic Hypoketotic Hypoglycemia Due to an AKT2 Mutation.
Garg N; Bademci G; Foster J; Sıklar Z; Berberoglu M; Tekin M
J Pediatr; 2015 Aug; 167(2):489-91. PubMed ID: 26003998
[TBL] [Abstract][Full Text] [Related]
3. Morfan: a new syndrome characterized by mental retardation, pre- and postnatal overgrowth, remarkable face and acanthosis nigricans in 5-year-old boy.
Seemanová E; Rüdiger HW; Dreyer M
Am J Med Genet; 1993 Feb; 45(4):525-8. PubMed ID: 8465862
[No Abstract] [Full Text] [Related]
4. CKAP2L mutation confirms the diagnosis of Filippi syndrome.
Capecchi G; Baldassarri M; Ferranti S; Guidoni E; Cioni M; Nürnberg P; Mencarelli MA; Renieri A; Grosso S
Clin Genet; 2018 May; 93(5):1109-1110. PubMed ID: 29473684
[No Abstract] [Full Text] [Related]
5. Rabson-Mendenhall syndrome.
Parveen BA; Sindhuja R
Int J Dermatol; 2008 Aug; 47(8):839-41. PubMed ID: 18717867
[TBL] [Abstract][Full Text] [Related]
6. Expanding the phenotype of Filippi Syndrome: a patient with early onset puberty.
Sabir A; Walker JK; Hart R
Clin Dysmorphol; 2019 Oct; 28(4):224-226. PubMed ID: 30921095
[No Abstract] [Full Text] [Related]
7. Myhre syndrome with facial paralysis and branch pulmonary stenosis.
Hawkes L; Kini U
Clin Dysmorphol; 2015 Apr; 24(2):84-5. PubMed ID: 25486016
[No Abstract] [Full Text] [Related]
8. Polyvalvular heart disease associated with short stature, facial anomalies, and mental retardation: an additional familial report.
Digilio MC; Capolino R; Versacci P; Marino B
Am J Med Genet A; 2004 May; 127A(1):101-103. PubMed ID: 15103728
[No Abstract] [Full Text] [Related]
9. Severe constipation in a patient with Myhre syndrome: a case report.
Bassett JK; Douzgou S; Kerr B
Clin Dysmorphol; 2016 Apr; 25(2):54-7. PubMed ID: 26636501
[TBL] [Abstract][Full Text] [Related]
10. [Acanthosis nigricans in children and Crouzon syndrome].
Lagaude M; Barreau M; Jokic M; Gerard M; DiRocco F; Hadj-Rabia S; Dompmartin A; Verneuil L
Ann Dermatol Venereol; 2014 Nov; 141(11):685-8. PubMed ID: 25442473
[TBL] [Abstract][Full Text] [Related]
11. Crouzon with acanthosis nigricans. Further delineation of the syndrome.
Arnaud-López L; Fragoso R; Mantilla-Capacho J; Barros-Núñez P
Clin Genet; 2007 Nov; 72(5):405-10. PubMed ID: 17935505
[TBL] [Abstract][Full Text] [Related]
12. [What's your diagnosis? Lichenification of flexures, tetraspasm and mental retardation].
Wachter T; Wesselmann U; Leverkus M; Heber U; Bröcker EB; Hamm H
Hautarzt; 2006 Aug; 57(8):708-10. PubMed ID: 16421762
[No Abstract] [Full Text] [Related]
13. A recessive disorder with growth and mental retardation, peculiar facies, abnormal pigmentation, hepatic cirrhosis and aminoaciduria.
Tay CH; Rajagopalan K; McEvoy-Bowe E; Tock EP; Da Costa JL
Acta Paediatr Scand; 1974 Sep; 63(5):777-82. PubMed ID: 4471978
[No Abstract] [Full Text] [Related]
14. Johanson-blizzard syndrome.
Godbole K; Maja S; Leena H; Martin Z
Indian Pediatr; 2013 May; 50(5):510-2. PubMed ID: 23778732
[TBL] [Abstract][Full Text] [Related]
15. [Acanthosis nigricans. II. Benign acanthosis nigricans].
Ollendorff-Curth H
Dermatol Monatsschr; 1975 Feb; 161(2):89-96. PubMed ID: 1213227
[No Abstract] [Full Text] [Related]
16. Mental retardation, short stature and brittle hair (BIDS syndrome; hair brain syndrome).
Hora RK; Murthy VS
Indian J Pediatr; 1996; 63(1):117-20. PubMed ID: 10829976
[No Abstract] [Full Text] [Related]
17. Generalised acanthosis nigricans in childhood with short stature associated with poor response to growth hormone provocation.
Iwade M; Ogawa E; Koga H; Mizuno F; Koike K; Matsumoto K; Okuyama R
Acta Derm Venereol; 2014 Jul; 94(4):486-7. PubMed ID: 24285118
[No Abstract] [Full Text] [Related]
18. Familial acanthosis nigricans.
Tasjian D; Jarratt M
Arch Dermatol; 1984 Oct; 120(10):1351-4. PubMed ID: 6486848
[TBL] [Abstract][Full Text] [Related]
19. A girl with 15q overgrowth syndrome and dup(15)(q24q26.3) that included telomeric sequences.
Gutiérrez-Franco Mde L; Madariaga-Campos Mde L; Vásquez-Velásquez AI; Matute E; Guevara-Yáñez R; Rivera H
Korean J Lab Med; 2010 Jun; 30(3):318-24. PubMed ID: 20603595
[TBL] [Abstract][Full Text] [Related]
20. Retinal involvement in two unrelated patients with Myhre syndrome.
Al Ageeli E; Mignot C; Afenjar A; Whalen S; Dorison N; Mayer M; Esteva B; Dubern B; Momtchilova M; Le Gargasson JF; Bursztyn J; Héron D
Eur J Med Genet; 2012 Oct; 55(10):541-7. PubMed ID: 22683461
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]