All individuals with variants in gene SP8

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00418596 Fam2PatIII1 PubMed: Bertoli-Avella 2022 3-generation family, 1 affected, unaffected heterozygous carrier parents/relatives M yes Bahrain Syria - - - - CF failure to thrive; prominent forehead, upslanting palpebral fissures, thin upper lips; normal motor development; normal mental development; no neurological abnormalities; recurrent lower respiratory tract infections; chronic coughing, pneumonia, hyperactive airway disease; no immunological abnormalities; acute gastroenteritis , vomiting, severe gastroesophag eal reflux, chronic diarrhea; no cardiovascular abnormalities 1 1 Johan den Dunnen
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