![My wife just gave birth to our firstborn, and me and my son both have the same weird genetic abnormality where we have an extra large space between our first and second My wife just gave birth to our firstborn, and me and my son both have the same weird genetic abnormality where we have an extra large space between our first and second](https://external-preview.redd.it/sd2Qci3gXfvdE9Bpf1vdl3yVJuZ6imYTC0OPnNnktPQ.jpg?auto=webp&s=d8986579531241fd35f319813f9caca8e761bcdb)
My wife just gave birth to our firstborn, and me and my son both have the same weird genetic abnormality where we have an extra large space between our first and second
![Phenotypic expansion of the BPTF‐related neurodevelopmental disorder with dysmorphic facies and distal limb anomalies - Glinton - 2021 - American Journal of Medical Genetics Part A - Wiley Online Library Phenotypic expansion of the BPTF‐related neurodevelopmental disorder with dysmorphic facies and distal limb anomalies - Glinton - 2021 - American Journal of Medical Genetics Part A - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/3b9360e7-85ed-4c58-b6d4-349a6766aafe/ajmga62102-fig-0003-m.jpg)
Phenotypic expansion of the BPTF‐related neurodevelopmental disorder with dysmorphic facies and distal limb anomalies - Glinton - 2021 - American Journal of Medical Genetics Part A - Wiley Online Library
![Pathogenic nonsense variant in NFIB in another patient with dysmorphism, Autism Spectrum Disorder, agenesis of the corpus callosum, and intellectual disability - ScienceDirect Pathogenic nonsense variant in NFIB in another patient with dysmorphism, Autism Spectrum Disorder, agenesis of the corpus callosum, and intellectual disability - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S1769721220308028-gr1.jpg)
Pathogenic nonsense variant in NFIB in another patient with dysmorphism, Autism Spectrum Disorder, agenesis of the corpus callosum, and intellectual disability - ScienceDirect
MDUMC REACH 2k15 - #Do you know? This is SANDAL GAP... The Gap between the first and second toes A typical feature of DOWN'S SYNDROME | Facebook
![Nicolaides–Baraitser syndrome: Delineation of the phenotype - Sousa - 2009 - American Journal of Medical Genetics Part A - Wiley Online Library Nicolaides–Baraitser syndrome: Delineation of the phenotype - Sousa - 2009 - American Journal of Medical Genetics Part A - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/c584496f-fa04-4f24-816b-e8c65cc4d309/mfig004.jpg)