Cleft palate-large ears-small head syndrome

Cleft palate-large ears-small head syndrome is a rare, genetic syndrome characterized by cleft palate, large protruding ears, microcephaly and short stature (prenatal onset). Other skeletal abnormalities (delayed bone age, distally tapering fingers, hypoplastic distal phalanges, proximally placed thumbs, fifth finger clinodactyly), Pierre Robin sequence, cystic renal dysplasia, proximal renal tubular acidosis, hypospadias, cerebral anomalies on imaging (enlargement of lateral ventricles, mild cortical atrophy), seizures, hypotonia and developmental delay are also observed.



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Total: 0 (papers)

  


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Matched Phenotype  Gene  Mutation  MeSH
Rank
(Similarity)
PMID
(PMCID)
        

Phenotype(s) retrieved from Orphanet

    Total: 19

HPO ID Term Frequency
HP:0000175 Cleft palate Very frequent (99-80%)
HP:0000252 Microcephaly Very frequent (99-80%)
HP:0000400 Macrotia Very frequent (99-80%)
HP:0002750 Delayed skeletal maturation Very frequent (99-80%)
HP:0004322 Short stature Very frequent (99-80%)
HP:0000047 Hypospadias Frequent (79-30%)
HP:0000212 Gingival overgrowth Frequent (79-30%)
HP:0000347 Micrognathia Frequent (79-30%)
HP:0000411 Protruding ear Frequent (79-30%)
HP:0000508 Ptosis Frequent (79-30%)
HP:0000767 Pectus excavatum Frequent (79-30%)
HP:0001252 Muscular hypotonia Frequent (79-30%)
HP:0001263 Global developmental delay Frequent (79-30%)
HP:0001800 Hypoplastic toenails Frequent (79-30%)
HP:0003202 Skeletal muscle atrophy Frequent (79-30%)
HP:0004428 Elfin facies Frequent (79-30%)
HP:0006709 Aplasia/Hypoplasia of the nipples Frequent (79-30%)
HP:0009465 Ulnar deviation of finger Frequent (79-30%)
HP:0009882 Short distal phalanx of finger Frequent (79-30%)


Phenotype(s) retrieved from case reports

    Total: 0

HPO ID Term # of case reports


Causative gene(s) retrieved from Orphanet

    Total: 0

Gene Symbol Gene Name Entrez Gene ID