Rare Diseases Symptoms Automatic Extraction

Clinical Features in Patients With 22q11.2 Deletion Syndrome Ascertained by Palatal Abnormalities.

[22q11.2 deletion syndrome]

Objectives :  The aim of this study was to describe clinical features in subjects with palatal abnormalities and to assess the distribution of these features among those with and without 22q11.2 deletion. Design :  Descriptive cohort. Patients :  One hundred patients with palatal abnormalities and suspicion of 22q11.2 DS were included. Methods :  All patients were evaluated by a clinical geneticist, who completed a standardized clinical protocol. The 22q11.2 deletion screening was performed with fluorescence in situ hybridization using the TUPLE1 probe and multiplex ligation-dependent probe amplification using the P250-A1 kit. Results :  The 22q11.2 deletion was detected in 35 patients, in whom the most frequent clinical features were congenital heart disease (50%), developmental delay (54%), speech delay (57%), learning disabilities (77%), and immunologic alterations/recurrent infections (62%). In addition, the most common facial dysmorphisms in this group were long face (77%), typical nose (69%), and hooded eyelids (54%). Comparing features in patients with or without the deletion revealed significant differences (positively correlated with the deletion) for speech delay, learning disabilities, conductive hearing loss, number of dysmorphisms, long face, and hooded eyelids. Cleft lip and palate was negatively correlated with the deletion. Conclusions :  The presence of speech delay, learning disabilities, conductive hearing loss, long face, and hooded eyelids should reinforce the suspicion of 22q11.2 DS in patients with palatal abnormalities and would help professionals direct clinical follow-up of these patients.

Diseases presenting "heart disease" symptom

  • 22q11.2 deletion syndrome
  • achondroplasia
  • acute rheumatic fever
  • adrenal incidentaloma
  • child syndrome
  • classical phenylketonuria
  • cohen syndrome
  • congenital diaphragmatic hernia
  • dentinogenesis imperfecta
  • esophageal adenocarcinoma
  • fabry disease
  • familial mediterranean fever
  • heparin-induced thrombocytopenia
  • hirschsprung disease
  • holt-oram syndrome
  • homocystinuria without methylmalonic aciduria
  • kabuki syndrome
  • monosomy 21
  • omenn syndrome
  • phenylketonuria
  • sneddon syndrome
  • systemic capillary leak syndrome
  • wiskott-aldrich syndrome
  • wolf-hirschhorn syndrome

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