Seckel syndrome with Morgagni hernia

Clinical Dysmorphology

Volumn 16, Issue 3, 2007, Pages 209-210

  Onder, Asan ^a   Cogulu, Ozgur ^a   Ekmekci, Aslihan ^a   Pariltay, Erhan ^a   Kirbiyik, Ozgur ^a   Ozkinay, Ferda ^a  

^a EGE UNIVERSITY   (Turkey)

Author keywords

Microcephalic dwarfism; Morgagni hernia; Seckel syndrome

Indexed keywords

ARTICLE; CASE REPORT; CLINICAL FEATURE; CLINODACTYLY; COMPUTER ASSISTED TOMOGRAPHY; DIAPHRAGM HERNIA; DISEASE ASSOCIATION; EAR MALFORMATION; FACE ASYMMETRY; FACE MALFORMATION; FAILURE TO THRIVE; HUMAN; HYPOSPADIAS; MALE; MENTAL DEFICIENCY; MICROCEPHALY; MORGAGNI HERNIA; NOSE MALFORMATION; NUCLEAR MAGNETIC RESONANCE IMAGING; PHYSICAL EXAMINATION; PRESCHOOL CHILD; PRIORITY JOURNAL; RADIODIAGNOSIS; SECKEL SYNDROME; SKELETON MALFORMATION; THORAX RADIOGRAPHY;

ABNORMALITIES, MULTIPLE; CHILD, PRESCHOOL; HERNIA, DIAPHRAGMATIC; HUMANS; MALE; SYNDROME;

EID: 34249984722     PISSN: 09628827     EISSN: None     Source Type: Journal    
DOI: 10.1097/MCD.0b013e3281c9b08e     Document Type: Article

References (6)

1. Bangstad HJ, Beck-Nielsen H, Hother Nielsen O, Nystad R, Trygstad O, Pedersen O, Aagenaes O (1989). Primordial bird headed nanism associated with progressive ataxia, early onset insulin resistant diabetes, goiter, and primary gonadal insufficiency. Acta Paediat Scand 78:488-493.
2. Cohen MM Jr (1991). Hallermann-Streiff syndrome: a review. Am J Med Genet 41:488-499.
3. Doerfler W, Wieczorek D, Gillessen-Kaesbach G, Albrecht B, Passarge E (1997). Three brothers with mental and physical retardation, hydrocephalus, microcephaly, internal malformations, speech disorder, and facial anomalies Mutchinick syndrome. Am J Med Genet 73:210-216.
4. Harper RG, Orti E, Baker RK (1967). Bird-beaded dwarfs (Seckel's syndrome). A familial pattern of developmental, dental, skeletal, genital, and central nervous system anomalies. J Pediatr 70:799-804.
5. Hartman GE (2004). Diaphragmatic hernia. In: Behrman RE, Kliegman RM, Jenson HB (editors). Nelson textbook of pediatrics. 17th ed. pp. 1353-1355.
6. Woods CG, Leversha M, Rogers JG (1995). Severe intrauterine growth retardation with increased mitomycin C sensitivity: a further chromosome breakage syndrome. J Med Genet 32:301-305.