Disease #07094 (APMR (alopecia-mental retardation syndrome))

Official abbreviation APMR
Name alopecia-mental retardation syndrome
OMIM ID -
Inheritance -
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene LSS
Associated tissues -
Disease features -
Remarks -
Date created 2024-06-28 15:12:57 +02:00 (CEST)
Date last edited N/A


Individuals

1 entry on 1 page. Showing entry 1.
Legend   How to query  

AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Genes screened

Variants in genes

Variants     

Panel size     

Owner     
00451687 patient PubMed: Elaraby 2022, Journal: Elaraby 2022 4-generation family, 3 affected sibs (2F, fetus) F yes Egypt - - - - - APMR see paper; ...,respiratory distress; complete hair loss scalp, eyelashes, eyebrows; microcephalic (OFC -2.3 SD), normal weight, normal height; developmental delay; facial dysmorphism; short stature; growth retardation; umbilical hernia; hyperextensibility joints; tooth mineralization defect; dental deep overbite LSS LSS 1 3 Nesma M. Elaraby
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.