Seckel syndrome - Misplaced Pages

(Redirected from Virchow-Seckel syndrome) Medical condition

Seckel syndrome
Other names	Harper's syndrome

Boy with Seckel syndrome (left)
Specialty	Medical genetics
Causes	defects of genes on chromosome 3 and 18.

Seckel syndrome, or microcephalic primordial dwarfism (also known as bird-headed dwarfism, Harper's syndrome, Virchow–Seckel dwarfism and bird-headed dwarf of Seckel) is an extremely rare congenital nanosomic disorder. Inheritance is autosomal recessive. It is characterized by intrauterine growth restriction and postnatal dwarfism with a small head, narrow bird-like face with a beak-like nose, large eyes with down-slanting palpebral fissures, receding mandible and intellectual disability.

A mouse model has been developed. This mouse model is characterized by a severe deficiency of ATR protein. These mice have high levels of replicative stress and DNA damage. Adult Seckel mice display accelerated aging. These findings are consistent with the DNA damage theory of aging.

Symptoms and signs

Symptoms include:

intellectual disability (more than half of the patients have an IQ below 50)
microcephaly
sometimes pancytopenia (low blood counts)
cryptorchidism in males
low birth weight
dislocations of pelvis and elbow
unusually large eyes
blindness or visual impairment
large, low-set ears
small chin due to receded lower jaw

Genetics

It is believed to be caused by defects of genes on chromosome 3 and 18. One form of Seckel syndrome can be caused by mutation in the gene encoding the ataxia telangiectasia and Rad3-related protein (ATR) which maps to chromosome 3q22.1–q24. This gene is central in the cell's DNA damage response and repair mechanism.

Types include:

Type	OMIM	Gene	Locus
SCKL1	210600	ATR	3q23
SCKL2	606744	RBBP8	18q11
SCKL4	613676	CENPJ	13q12
SCKL5	613823	CEP152	15q21.1
SCKL6	614728	CEP63	3q22.2
SCKL7	614851	NIN	14q22.1
SCKL8	615807	DNA2	10q21.3
SCKL9	616777	TRAIP	3p21.31
SCKL10	617253	NSMCE2	8q24.13
SCKL11	620767	CEP295	11q21

Diagnosis

There are 4 criteria for diagnosis:

Congenital Dwarfism and postnatal growth retardation
Microcephaly, large eyes, beak-like nose, narrow face, retrognathism, malocclusion
Mental handicap
Agenesis of the corpus callosum, cerebral cysts

Other abnormalities can be a supportive criteria, such as: anemia, pancytopenia, cleft lip/palate scoliosis or kyphoscoliosis.

Genetic testing can confirm diagnosis.

Treatment

There is no cure for Seckel syndrome. Symptomatic treatment is available.

History

The syndrome was named after German–American physician Helmut Paul George Seckel (1900–1960). The synonym Harper's syndrome was named after pediatrician Rita G. Harper.

References

Harsha Vardhan BG, Muthu MS, Saraswathi K, Koteeswaran D (2007). "Bird-headed dwarf of Seckel". J Indian Soc Pedod Prev Dent. 25 Suppl: S8–9. PMID 17921644.
James Wynbrandt; Mark D. Ludman (February 2008). The encyclopedia of genetic disorders and birth defects. Infobase Publishing. pp. 344–. ISBN 978-0-8160-6396-3. Retrieved 7 January 2011.
Jung M, Rai A, Wang L, Puttmann K, Kukreja K, Koh CJ (2018). "Nephrolithiasis in a 17-Year-Old Male With Seckel Syndrome and Horseshoe Kidneys: Case Report and Review of the Literature". Urology. 120: 241–243. doi:10.1016/j.urology.2018.05.023. PMID 29894776. S2CID 48353132.
^ Murga M, Bunting S, Montaña MF, et al. (August 2009). "A mouse model of ATR-Seckel shows embryonic replicative stress and accelerated aging". Nat. Genet. 41 (8): 891–8. doi:10.1038/ng.420. PMC 2902278. PMID 19620979.
^ "Seckel Syndrome - Symptoms, Causes, Treatment | NORD". rarediseases.org. Retrieved 2025-01-10.
"Entry - #210600 - SECKEL SYNDROME 1; SCKL1 - OMIM". omim.org. Retrieved 2025-01-10.
Bissonnette, Bruno; Luginbuehl, Igor; Engelhardt, Thomas (2019), "Seckel Syndrome", Syndromes: Rapid Recognition and Perioperative Implications (2 ed.), New York, NY: McGraw-Hill Education, retrieved 2025-01-10
Bissonnette, Bruno; Luginbuehl, Igor; Engelhardt, Thomas (2019), "Seckel Syndrome", Syndromes: Rapid Recognition and Perioperative Implications (2 ed.), New York, NY: McGraw-Hill Education, retrieved 2025-01-10
"Seckel Syndrome - Symptoms, Causes, Treatment | NORD". rarediseases.org. Retrieved 2025-01-10.
Kelana, Andreas Dhymas Dhyna Martha; Windiani, Gusti Ayu Trisna; Arimbawa, Made; Adnyana, Gusti Agung Ngurah Sugitha; Yuda, Made Darma; Murti, Ni Luh Sukma Pratiwi; Soetjiningsih, Soetjiningsih (2023-01-04). "Case of Seckel Syndrome in a 9-month-old Girl". Open Access Macedonian Journal of Medical Sciences. 11 (C): 6–10. doi:10.3889/oamjms.2023.10988. ISSN 1857-9655.
Seckel, H. P. G. Bird-headed Dwarfs: Studies in Developmental Anthropology Including Human Proportions. Springfield, Ill.: Charles C Thomas (pub.) 1960.
"Seckel's syndrome".
Harper RG, Orti E, Baker RK (May 1967). "Bird-beaded dwarfs (Seckel's syndrome). A familial pattern of developmental, dental, skeletal, genital, and central nervous system anomalies". J. Pediatr. 70 (5): 799–804. doi:10.1016/S0022-3476(67)80334-2. PMID 6022184.

External links

Seckel's syndrome at Who Named It?

Classification	D ICD-10: Q87.1 ICD-9-CM: 759.89 OMIM: 210600 DiseasesDB: 31625
External resources	Orphanet: 808

v t e Congenital abnormality syndromes
Craniofacial	Acrocephalosyndactyly Apert syndrome Carpenter syndrome Pfeiffer syndrome Saethre–Chotzen syndrome Sakati–Nyhan–Tisdale syndrome Bonnet–Dechaume–Blanc syndrome Other Baller–Gerold syndrome Cyclopia Goldenhar syndrome Moebius syndrome Pierre Robin sequence
Short stature	1q21.1 deletion syndrome Aarskog–Scott syndrome Cockayne syndrome Cornelia de Lange syndrome Dubowitz syndrome Noonan syndrome Robinow syndrome Silver–Russell syndrome Seckel syndrome Smith–Lemli–Opitz syndrome Snyder–Robinson syndrome Turner syndrome
Limbs	Adducted thumb syndrome Holt–Oram syndrome Klippel–Trénaunay syndrome Nail–patella syndrome Rubinstein–Taybi syndrome Gastrulation/mesoderm: Caudal regression syndrome Ectromelia Sirenomelia VACTERL association
Overgrowth syndromes	Bannayan–Riley–Ruvalcaba syndrome Beckwith–Wiedemann syndrome Benign symmetric lipomatosis Klippel–Trénaunay syndrome Neurofibromatosis type I Perlman syndrome Proteus syndrome Sotos syndrome Tatton-Brown–Rahman syndrome Weaver syndrome
Laurence–Moon–Bardet–Biedl	Bardet–Biedl syndrome Laurence–Moon syndrome
Combined/other, known locus	2 (Feingold syndrome) 3 (Zimmermann–Laband syndrome) 4/13 (Fraser syndrome) 8 (Branchio-oto-renal syndrome, CHARGE syndrome) 12 (Keutel syndrome, Timothy syndrome) 15 (Marfan syndrome) 19 (Donohue syndrome) Multiple Fryns syndrome

Deficiencies of intracellular signaling peptides and proteins

GTP-binding protein regulators

GTPase-activating protein	Neurofibromatosis type I Watson syndrome Tuberous sclerosis
Guanine nucleotide exchange factor	Marinesco–Sjögren syndrome Aarskog–Scott syndrome Juvenile primary lateral sclerosis X-linked intellectual disability 1

G protein

Heterotrimeic

Monomeric

RAS: HRAS
- Costello syndrome
KRAS
- Noonan syndrome 3
- KRAS Cardiofaciocutaneous syndrome

RAB: RAB7
- Charcot–Marie–Tooth disease
RAB23
- Carpenter syndrome
RAB27
- Griscelli syndrome type 2

RHO: RAC2
- Neutrophil immunodeficiency syndrome

MAP kinase

Cardiofaciocutaneous syndrome

Other kinase/phosphatase

Tyrosine kinase	BTK X-linked agammaglobulinemia ZAP70 ZAP70 deficiency
Serine/threonine kinase	RPS6KA3 Coffin-Lowry syndrome CHEK2 Li–Fraumeni syndrome 2 IKBKG Incontinentia pigmenti STK11 Peutz–Jeghers syndrome DMPK Myotonic dystrophy 1 ATR Seckel syndrome 1 GRK1 Oguchi disease 2 WNK4/WNK1 Pseudohypoaldosteronism 2
Tyrosine phosphatase	PTEN Bannayan–Riley–Ruvalcaba syndrome Lhermitte–Duclos disease Cowden syndrome Proteus-like syndrome MTM1 X-linked myotubular myopathy PTPN11 Noonan syndrome 1 LEOPARD syndrome Metachondromatosis

Signal transducing adaptor proteins

Other

NF2
- Neurofibromatosis type II
Notch 3
- CADASIL
PRKAR1A
- Carney complex
PRKAG2
- Wolff–Parkinson–White syndrome
PRKCSH
- PRKCSH Polycystic liver disease
XIAP
- XIAP2

See also intracellular signaling peptides and proteins

v t e Nucleus diseases
Telomere	Revesz syndrome
Nucleolus	Treacher Collins syndrome Spinocerebellar ataxia 7 Cajal body: Spinal muscular atrophy
Centromere	CENPJ Seckel syndrome 4
Other	AAAS Triple-A syndrome Laminopathy SMC1A/SMC3 Cornelia de Lange Syndrome SETBP1 Schinzel–Giedion syndrome
see also nucleus

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