TY - JOUR
T1 - Focal dermal hypoplasia resulting from a new nonsense mutation, p.E300X, in the PORCN gene
AU - Clements, Suzanne E.
AU - Wessagowit, Vesarat
AU - Lai-Cheong, Joey E.
AU - Arita, Ken
AU - McGrath, John A.
PY - 2008/1
Y1 - 2008/1
N2 - Background: Focal dermal hypoplasia (FDH) (OMIM 305600) is an X-linked dominant disorder of ecto-mesodermal development. Also known as Goltz syndrome, FDH presents with characteristic linear streaks of hypoplastic dermis and variable abnormalities of bone, nails, hair, limbs, teeth and eyes. The molecular basis of FDH involves mutations in the PORCN gene, which encodes an enzyme that allows membrane targeting and secretion of several Wnt proteins critical for normal tissue development. Objectives: To investigate the molecular basis of FDH in a 2-year-old Thai girl who presented at birth with depressed, pale linear scars on the trunk and limbs, sparse brittle hair, syndactyly of the right middle and ring fingers, dental caries and radiological features of osteopathia striata. Methods: Sequencing of genomic DNA from the affected individual and both parents to search for pathogenic mutations in PORCN gene. Results: DNA sequencing disclosed a heterozygous G > T substitution at nucleotide c.898 within exon 10 (NM_203475.1), converting a glutamic acid residue (GAA) to a premature termination codon (TAA). This mutation, designated p.E300X, was not detected in DNA from either parent or in 100 control chromosomes. Conclusion: Identification of this new de novo nonsense mutation confirms the diagnosis of FDH in this child and highlights the clinical importance of PORCN and Wnt signalling pathways in embryogenesis.
AB - Background: Focal dermal hypoplasia (FDH) (OMIM 305600) is an X-linked dominant disorder of ecto-mesodermal development. Also known as Goltz syndrome, FDH presents with characteristic linear streaks of hypoplastic dermis and variable abnormalities of bone, nails, hair, limbs, teeth and eyes. The molecular basis of FDH involves mutations in the PORCN gene, which encodes an enzyme that allows membrane targeting and secretion of several Wnt proteins critical for normal tissue development. Objectives: To investigate the molecular basis of FDH in a 2-year-old Thai girl who presented at birth with depressed, pale linear scars on the trunk and limbs, sparse brittle hair, syndactyly of the right middle and ring fingers, dental caries and radiological features of osteopathia striata. Methods: Sequencing of genomic DNA from the affected individual and both parents to search for pathogenic mutations in PORCN gene. Results: DNA sequencing disclosed a heterozygous G > T substitution at nucleotide c.898 within exon 10 (NM_203475.1), converting a glutamic acid residue (GAA) to a premature termination codon (TAA). This mutation, designated p.E300X, was not detected in DNA from either parent or in 100 control chromosomes. Conclusion: Identification of this new de novo nonsense mutation confirms the diagnosis of FDH in this child and highlights the clinical importance of PORCN and Wnt signalling pathways in embryogenesis.
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U2 - 10.1016/j.jdermsci.2007.09.004
DO - 10.1016/j.jdermsci.2007.09.004
M3 - Article
C2 - 17951029
AN - SCOPUS:37049029018
SN - 0923-1811
VL - 49
SP - 39
EP - 42
JO - Journal of Dermatological Science
JF - Journal of Dermatological Science
IS - 1
ER -