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Premature posterior fontanelle closure

MedGen UID:
326407
Concept ID:
C1839126
Finding
HPO: HP:0005494

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVPremature posterior fontanelle closure

Conditions with this feature

Trigonocephaly-short stature-developmental delay syndrome
MedGen UID:
374138
Concept ID:
C1839125
Disease or Syndrome
Syndrome with characteristics of short stature, trigonocephaly and developmental delay. It has been described in three males. Moderate intellectual deficit was reported in one of the males and the other two patients displayed psychomotor retardation. X-linked transmission has been suggested but autosomal recessive inheritance cannot be ruled out.

Recent clinical studies

Etiology

Direk M, Makharoblıdze K, Polat BG, Özdemir AA, Okuyaz Ç
Turk J Med Sci 2022 Aug;52(4):934-941. Epub 2022 Aug 10 doi: 10.55730/1300-0144.5393. PMID: 36326403Free PMC Article
Sarigecili E, Makharoblidze K, Çobanogullari MD, Yildirim DD, Komur M, Okuyaz C
Childs Nerv Syst 2021 Feb;37(2):561-566. Epub 2020 Jul 31 doi: 10.1007/s00381-020-04846-6. PMID: 32737565
Sanchez-Lara PA, Graham JM Jr, Hing AV, Lee J, Cunningham M
Am J Med Genet A 2007 Dec 15;143A(24):3243-51. doi: 10.1002/ajmg.a.32073. PMID: 18000970

Diagnosis

Bellary SS, Steinberg A, Mirzayan N, Shirak M, Tubbs RS, Cohen-Gadol AA, Loukas M
Clin Anat 2013 Nov;26(8):922-7. Epub 2013 Aug 20 doi: 10.1002/ca.22262. PMID: 23959948
Sanchez-Lara PA, Graham JM Jr, Hing AV, Lee J, Cunningham M
Am J Med Genet A 2007 Dec 15;143A(24):3243-51. doi: 10.1002/ajmg.a.32073. PMID: 18000970

Clinical prediction guides

Direk M, Makharoblıdze K, Polat BG, Özdemir AA, Okuyaz Ç
Turk J Med Sci 2022 Aug;52(4):934-941. Epub 2022 Aug 10 doi: 10.55730/1300-0144.5393. PMID: 36326403Free PMC Article

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