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Form 1556-1A FWS Form 3-2350 rev 6/10 Date: UNITED STATES DOI BLM June 2012 PMDS PUBLICATIONS REQUISITION FORM FOR USFW TO: BLM/PMDS, SC-657B OFC: FTS/COM 303-236-1975/7637 DFC, BUILDING 41 Ent E16.

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These organs represent MD structures (the uterus, Fallopian tubes, and upper two-thirds of the vagina). However, radiological findings only revealed the right Fallopian tube in this syndrome (Fig. 3) [9]. PMDS patients are rarely fertile and most of them usually suffer from infertility and inguinal hernia.

Adult males with PMDS may be unable to biologically father children. Men with PMDS may also notice blood in their semen. They also have a higher risk of testicular cancer. More specifically, undescended testes left untreated may break down and develop cancer.

The first noted signs and symptoms in males with PMDS are usually undescended testes (cryptorchidism) or soft out-pouchings in the lower abdomen (inguinal hernias). The uterus and fallopian tubes are typically discovered when surgery is performed to treat these conditions.

These ducts typically regress in males under the influence of Anti-Müllerian Hormone (AMH), also known as Müllerian Inhibiting Substance (MIS), Müllerian Inhibiting Hormone (MIH), or Anti-Müllerian Factor (AMF).

Persistent Mullerian Duct Syndrome (PMDS) is a very rare condition with less than 300 cases described in the literature (1, 2). This rare entity showcases adolescents who are phenotypically males with 46,XY karyotypes.

Persistent Müllerian duct syndrome (PMDS) is a rare disease that occurs in men with a completely normal phenotype and is characterised by the presence of Müllerian duct structures. Organogenesis of the male external genitalia is not affected.

Persistent Mullerian duct syndrome (PMDS) is a rare disorder. It is a type of male pseudohermaphroditism, usually presenting as “Hernia Uteri Inguinalis”.

Persistent Mullerian duct syndrome (PMDS) is a rare form of internal male pseudohermaphroditism in which Mullerian duct derivatives are seen in a male patient. [1] The syndrome is caused either by an insufficient amount of Mullerian inhibiting factor (MIF) or due to insensitivity of the target organ to MIF.

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Form Packages
Adoption
Bankruptcy
Contractors
Divorce
Home Sales
Employment
Identity Theft
Incorporation
Landlord Tenant
Living Trust
Name Change
Personal Planning
Small Business
Wills & Estates
Packages A-Z
Form Categories
Affidavits
Bankruptcy
Bill of Sale
Corporate - LLC
Divorce
Employment
Identity Theft
Internet Technology
Landlord Tenant
Living Wills
Name Change
Power of Attorney
Real Estate
Small Estates
Wills
All Forms
Forms A-Z
Form Library
Customer Service
Terms of Service
DMCA Policy
About Us
Blog
Affiliates
Contact Us
Privacy Notice
Delete My Account
Site Map
All Forms
Search all Forms
Industries
Forms in Spanish
Localized Forms
Legal Guides
Real Estate Handbook
All Guides
Prepared for You
Notarize
Incorporation services
Our Customers
For Consumers
For Small Business
For Attorneys
Our Sites
US Legal Forms
USLegal
FormsPass
pdfFiller
signNow
airSlate workflows
DocHub
Instapage
Social Media
Call us now toll free:
1-877-389-0141
As seen in:
  • USA Today logo picture
  • CBC News logo picture
  • LA Times logo picture
  • The Washington Post logo picture
  • AP logo picture
  • Forbes logo picture
© Copyright 1997-2025
airSlate Legal Forms, Inc.
3720 Flowood Dr, Flowood, Mississippi 39232