Disease #00776 (BFLS (Borjeson-Forssman-Lehmann syndrome (BFLS)), OMIM:301900)

Official abbreviation BFLS
Name Borjeson-Forssman-Lehmann syndrome (BFLS)
OMIM ID 301900
Human Phenotype Ontology Project (HPO) HPO
Inheritance X-linked recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene PHF6
Associated tissues -
Disease features deep-set eyes, large ears with large lobes; global developmental delay (HP:0001263); intellectual disability (HP:0001249); seizure (HP:0001250); hypotonia (HP:0001252); short stature (HP:0004322); obesity (HP:0001513); digital abnormalities (HP_0011297); tapering fingers, rather hypoplastic external genitalia with pubertal delay
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2023-01-03 20:06:20 +01:00 (CET)


Individuals

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00405783 194266 - - M no Germany - - - - - BFLS Global developmental delay, Motor delay, Hypotonia, Infantile muscular hypotonia, Strabismus, Hypoglycemia, Neonatal hypoglycemia, Esodeviation, Patent foramen ovale, Constipation, Atrial septal defect, Plagiocephaly, Abnormality of calvarial morphology, Abnormal corpus callosum morphology, Agenesis of corpus callosum, Aplasia/Hypoplasia of the corpus callosum, Sleep disturbance, Sleep apnea, Abnormal testis morphology, Retractile testis, Lacrimal duct stenosis, Nasolacrimal duct obstruction PHF6 PHF6 1 1 Andreas Laner
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