Table 1. The progeroid syndromes.

Syndrome	Gene
Branchiooculofacial Syndrome	TFAP2A
Acromicric Dysplasia	FBN1
Ataxia-Telangiectasia	ATM
Bloom Syndrome	BLM
Cockayne Syndrome	ERCC6
Dyskeratosis Congenita	TERC
Fanconi Anemia	FANCA
Fontaine Syndrome	SLC25A24
GAPO Syndrome	ANTXR1
Geroderma Osteodysplasticum	GORAB
Hutchison-Gilford Progeria Syndrome	LMNA
Keppen-Lubinsky Syndrome	KCNJ6
Mandibular hypoplasia, Deafness, Progeroid features, and Lipodystrophy Syndrome	POLD1
Marbach-Rustad Progeroid Syndrome	LEMD2
Nestor-Guillermo Progeria Syndrome	BANF1
Nijmegen breakage Syndrome	NBS1
Penttinen Syndrome	PDGFRB
Rahman Syndrome	HIST1H1E
Rothmund-Thomson Syndrome	RECQL4
Ruijs-Aalfs Syndrome	SPRTN
Saul-Wilson Syndrome	COG4
Seckel Syndrome	ATR
Seckel Syndrome 2	RBBP8
Short stature, Hyperextensibility, Hernia, Ocular depression, Rieger anomaly, and Teething delay Syndrome	PIK3R1
Werner Syndrome	WRN
Wiedemann-Rautenstrauch Syndrome	POLR3A
Xeroderma Pigmentosum group A	XPA
Xeroderma Pigmentosum group B	XPB
Xeroderma Pigmentosum group C	XPC
Xeroderma Pigmentosum group E	XPE
Xeroderma Pigmentosum group F	XPF
Xeroderma Pigmentosum group G	XPG
Xeroderma Pigmentosum group V	XPV

Table listing the progeroid syndromes by name and respective affected gene.