Cleft hard palate




Input patient's signs and symptoms


Narrow down the case reports



Total: 2 (papers)

   


(per page)
Matched Phenotype  Gene  Mutation  MeSH
Rank
(Similarity)		 PMID
(PMCID)
1
(59.0%)		 15103720
 Proximal chromosome 8q deletion in a boy with femoral bifurcation and other multiple congenital anomalies.
Asamoah A, Nwankwo M, Kumar SP, Ezhuthachan SG, Van Dyke DL.
Am J Med Genet A. 2004;127A(1):65-8.
Micrognathia Prominent forehead
Chromosome Deletion Chromosomes, Human, Pair 8 Femur Homo sapiens Infant, Newborn Male Spectral Karyotyping
2
(17.5%)		 22711197
 Free segmental vastus lateralis muscle flap for reconstruction of recalcitrant defects of the cleft hard palate.
Acarturk TO.
J Reconstr Microsurg. 2012;28(8):509-14.
Scarring
Child Cleft Palate Females Hard Palate Homo sapiens Reconstructive Surgical Procedures Repeat Surgery Suture Techniques
        

Phenotype(s) retrieved from Orphanet

    Total: 0

HPO ID Term Frequency


Phenotype(s) retrieved from case reports

    Total: 7

HPO ID Term # of case reports
HP:0000054 Micropenis 1
HP:0000316 Hypertelorism 1
HP:0000347 Micrognathia 1
HP:0000358 Posteriorly rotated ears 1
HP:0000470 Short neck 1
HP:0008110 Equinovarus deformity 1
HP:0011220 Prominent forehead 1


Causative gene(s) retrieved from Orphanet

    Total: 2

Gene Symbol Gene Name Entrez Gene ID
GRHL3 grainyhead like transcription factor 3 57822
UBB ubiquitin B 7314