1p36 deletion syndrome
1p36 deletion syndrome (also known as monosomy 1p36) is a congenital genetic disorder characterized by moderate to severe intellectual disability, delayed growth, hypotonia, seizures, limited speech ability, malformations, hearing and vision impairment, and distinct facial features. The symptoms may vary, depending on the exact location of the chromosomal deletion.
primaryTopic
1p36 deletion syndrome
1p36 deletion syndrome (also known as monosomy 1p36) is a congenital genetic disorder characterized by moderate to severe intellectual disability, delayed growth, hypotonia, seizures, limited speech ability, malformations, hearing and vision impairment, and distinct facial features. The symptoms may vary, depending on the exact location of the chromosomal deletion.
has abstract
1p36 deletion syndrome (also k ...... ernational medical literature.
@en
El síndrome de deleción o supr ...... ta de la deleción cromosómica.
@es
La Monosomie du chromosome 1 e ...... tade embryonnaire (4-5 jours).
@fr
Síndrome de Delecção do 1p36 ( ...... teratura médica internacional.
@pt
Zespół monosomii 1p36 (ang. mo ...... ótkiego ramienia chromosomu 1.
@pl
Link from a Wikipage to an external page
Wikipage page ID
Wikipage revision ID
695.598.386
Caption
A toddler showing facial symptoms of the syndrome.
DiseasesDB
OMIM
hypernym
type
comment
1p36 deletion syndrome (also k ...... n of the chromosomal deletion.
@en
El síndrome de deleción o supr ...... ta de la deleción cromosómica.
@es
La Monosomie du chromosome 1 e ...... tade embryonnaire (4-5 jours).
@fr
Síndrome de Delecção do 1p36 ( ...... nte a localização da delecção.
@pt
Zespół monosomii 1p36 (ang. mo ...... ótkiego ramienia chromosomu 1.
@pl
label
1p36 deletion syndrome
@en
Monosomie 1p36
@fr
Sindrome de deleção do 1p36
@pt
Síndrome de supresión 1p36
@es
Zespół monosomii 1p36
@pl
